{"database": "openregs", "table": "federal_register", "rows": [["2024-19414", "Medical Devices and Device-Led Combination Products; Voluntary Malfunction Summary Reporting for Manufacturers", "Rule", "The Food and Drug Administration (FDA, Agency, or we) is announcing a minor, technical modification to an alternative that permits manufacturer reporting of certain device malfunction medical device reports (MDRs) in summary form on a quarterly basis. We refer to this alternative as the \"Voluntary Malfunction Summary Reporting Program.\"", "2024-08-29", 2024, 8, "https://www.federalregister.gov/documents/2024/08/29/2024-19414/medical-devices-and-device-led-combination-products-voluntary-malfunction-summary-reporting-for", "https://www.govinfo.gov/content/pkg/FR-2024-08-29/pdf/2024-19414.pdf", "Health and Human Services Department; Food and Drug Administration", "221,199", "The Food and Drug Administration (FDA, Agency, or we) is announcing a minor, technical modification to an alternative that permits manufacturer reporting of certain device malfunction medical device reports (MDRs) in summary form on a quarterly basis....", null]], "columns": ["document_number", "title", "type", "abstract", "publication_date", "pub_year", "pub_month", "html_url", "pdf_url", "agency_names", "agency_ids", "excerpts", "regulation_id_numbers"], "primary_keys": ["document_number"], "primary_key_values": ["2024-19414"], "units": {}, "query_ms": 28.636754024773836, "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"}