{"database": "openregs", "table": "documents", "is_view": false, "human_description_en": "where docket_id = \"FDA-2017-D-5570\" sorted by posted_date descending", "rows": [["FDA-2017-D-5570-0020", "FDA", "FDA-2017-D-5570", "Recommendations for Clinical Laboratory Improvement Amendments of 1988 (CLIA) Waiver Applications for Manufacturers of In Vitro Diagnostic Devices Guidance for Industry and Food and Drug Administration Staff", "Other", "Guidance", "2020-02-26T05:00:00Z", 2020, 2, "2020-02-26T05:00:00Z", null, "2024-11-06T23:33:16Z", null, 1, 0, "09000064843b60b4"], ["FDA-2017-D-5570-0019", "FDA", "FDA-2017-D-5570", "Recommendations for Clinical Laboratory Improvement Amendments of 1988 Waiver Applications for Manufacturers of In Vitro Diagnostic Devices; Guidance for Industry and Food and Drug Administration Staff; Availability", "Notice", "Notice of Availability", "2020-02-26T05:00:00Z", 2020, 2, "2020-02-26T05:00:00Z", null, "2020-02-26T14:53:23Z", "2020-03860", 0, 0, "09000064843b4ec1"], ["FDA-2017-D-5570-0012", "FDA", "FDA-2017-D-5570", "Select Updates for Recommendations for Clinical Laboratory Improvement Amendments of 1988 Waiver Applications for Manufacturers of In Vitro Diagnostic Devices; Draft Guidance for Industry and Food and Drug Administration Staff; Availability", "Notice", "Notice of Availability", "2018-11-29T05:00:00Z", 2018, 11, "2018-11-29T05:00:00Z", "2019-02-28T04:59:59Z", "2024-11-12T22:50:46Z", "2018-25959", 1, 0, "090000648390c0fa"], ["FDA-2017-D-5570-0013", "FDA", "FDA-2017-D-5570", "Draft Guidance for Industry and FDA_Select Updates for CLIA of 1988 Waiver Applications for Manufacturers of IVD Devices_11-29-2018", "Other", "Guidance", "2018-11-29T05:00:00Z", 2018, 11, "2018-11-29T05:00:00Z", "2019-02-28T04:59:59Z", "2024-11-12T22:50:08Z", null, 1, 0, "090000648390cc70"], ["FDA-2017-D-5570-0006", "FDA", "FDA-2017-D-5570", "Select Updates for Recommendations for Clinical Laboratory Improvement Amendments of 1988 Waiver Applications for  Manufacturers of In Vitro Diagnostic Devices; Draft Guidance for Industry and Food and Drug Administration Staff; Availability; Extension of Comment Period", "Notice", "Notice of Availability", "2018-01-26T05:00:00Z", 2018, 1, "2018-01-26T05:00:00Z", "2018-03-31T03:59:59Z", "2018-03-31T01:01:21Z", "2018-01349", 0, 0, "0900006482e6be59"], ["FDA-2017-D-5570-0005", "FDA", "FDA-2017-D-5570", "Request for Extension from Coalition for CLIA Waiver Reform (Epstein Becker & Green, P.C.)", "Other", "Request for Extension", "2018-01-08T05:00:00Z", 2018, 1, "2018-01-08T05:00:00Z", null, "2018-01-08T16:20:10Z", null, 0, 0, "0900006482d9d48d"], ["FDA-2017-D-5570-0001", "FDA", "FDA-2017-D-5570", "Select Updates for Recommendations for Clinical Laboratory  Improvement Amendments of 1988 Waiver Applications for  Manufacturers of In Vitro Diagnostic Devices; Draft Guidance for Industry and Food and Drug Administration Staff; Availability", "Notice", "Notice of Availability", "2017-11-29T05:00:00Z", 2017, 11, "2017-11-29T05:00:00Z", "2018-01-30T04:59:59Z", "2018-01-14T03:27:08Z", "2017-25775", 0, 0, "0900006482cbbc77"], ["FDA-2017-D-5570-0002", "FDA", "FDA-2017-D-5570", "Select Updates for Recommendations for Clinical Laboratory  Improvement Amendments of 1988 (CLIA) Waiver Applications for Manufacturers of In Vitro Diagnostic Devices Draft Guidance for Industry and Food and Drug Administration Staff", "Other", "Guidance", "2017-11-29T05:00:00Z", 2017, 11, "2017-11-29T05:00:00Z", "2018-03-31T03:59:59Z", "2024-11-07T01:12:28Z", null, 1, 0, "0900006482cbce4e"]], "truncated": false, "filtered_table_rows_count": 8, "expanded_columns": [], "expandable_columns": [[{"column": "docket_id", "other_table": "dockets", "other_column": "id"}, "title"]], "columns": ["id", "agency_id", "docket_id", "title", "document_type", "subtype", "posted_date", "posted_year", "posted_month", "comment_start_date", "comment_end_date", "last_modified", "fr_doc_num", "open_for_comment", "withdrawn", "object_id"], "primary_keys": ["id"], "units": {}, "query": {"sql": "select id, agency_id, docket_id, title, document_type, subtype, posted_date, posted_year, posted_month, comment_start_date, comment_end_date, last_modified, fr_doc_num, open_for_comment, withdrawn, object_id from documents where \"docket_id\" = :p0 order by posted_date desc limit 101", "params": {"p0": "FDA-2017-D-5570"}}, "facet_results": {"agency_id": {"name": "agency_id", "type": "column", "hideable": false, "toggle_url": "/openregs/documents.json?docket_id=FDA-2017-D-5570", "results": [{"value": "FDA", "label": "FDA", "count": 8, "toggle_url": "https://www.pawtectors.org/openregs/documents.json?docket_id=FDA-2017-D-5570&agency_id=FDA", "selected": false}], "truncated": false}, "document_type": {"name": "document_type", "type": "column", "hideable": false, "toggle_url": "/openregs/documents.json?docket_id=FDA-2017-D-5570", "results": [{"value": "Notice", "label": "Notice", "count": 4, "toggle_url": "https://www.pawtectors.org/openregs/documents.json?docket_id=FDA-2017-D-5570&document_type=Notice", "selected": false}, {"value": "Other", "label": "Other", "count": 4, "toggle_url": "https://www.pawtectors.org/openregs/documents.json?docket_id=FDA-2017-D-5570&document_type=Other", "selected": false}], "truncated": false}, "posted_year": {"name": "posted_year", "type": "column", "hideable": false, "toggle_url": "/openregs/documents.json?docket_id=FDA-2017-D-5570", "results": [{"value": 2018, "label": 2018, "count": 4, "toggle_url": "https://www.pawtectors.org/openregs/documents.json?docket_id=FDA-2017-D-5570&posted_year=2018", "selected": false}, {"value": 2017, "label": 2017, "count": 2, "toggle_url": "https://www.pawtectors.org/openregs/documents.json?docket_id=FDA-2017-D-5570&posted_year=2017", "selected": false}, {"value": 2020, "label": 2020, "count": 2, "toggle_url": "https://www.pawtectors.org/openregs/documents.json?docket_id=FDA-2017-D-5570&posted_year=2020", "selected": false}], "truncated": false}}, "suggested_facets": [{"name": "subtype", "toggle_url": "https://www.pawtectors.org/openregs/documents.json?docket_id=FDA-2017-D-5570&_facet=subtype"}, {"name": "posted_date", "toggle_url": "https://www.pawtectors.org/openregs/documents.json?docket_id=FDA-2017-D-5570&_facet=posted_date"}, {"name": "posted_month", "toggle_url": "https://www.pawtectors.org/openregs/documents.json?docket_id=FDA-2017-D-5570&_facet=posted_month"}, {"name": "comment_start_date", "toggle_url": "https://www.pawtectors.org/openregs/documents.json?docket_id=FDA-2017-D-5570&_facet=comment_start_date"}, {"name": "comment_end_date", "toggle_url": "https://www.pawtectors.org/openregs/documents.json?docket_id=FDA-2017-D-5570&_facet=comment_end_date"}, {"name": "open_for_comment", "toggle_url": "https://www.pawtectors.org/openregs/documents.json?docket_id=FDA-2017-D-5570&_facet=open_for_comment"}, {"name": "posted_date", "type": "date", "toggle_url": "https://www.pawtectors.org/openregs/documents.json?docket_id=FDA-2017-D-5570&_facet_date=posted_date"}, {"name": "comment_start_date", "type": "date", "toggle_url": "https://www.pawtectors.org/openregs/documents.json?docket_id=FDA-2017-D-5570&_facet_date=comment_start_date"}, {"name": "comment_end_date", "type": "date", "toggle_url": "https://www.pawtectors.org/openregs/documents.json?docket_id=FDA-2017-D-5570&_facet_date=comment_end_date"}, {"name": "last_modified", "type": "date", "toggle_url": "https://www.pawtectors.org/openregs/documents.json?docket_id=FDA-2017-D-5570&_facet_date=last_modified"}], "next": null, "next_url": null, "private": false, "allow_execute_sql": true, "query_ms": 3562.465069000609, "source": "Federal Register API & Regulations.gov API", "source_url": "https://www.federalregister.gov/developers/api/v1", "license": "Public Domain (U.S. Government data)", "license_url": "https://www.regulations.gov/faq"}