{"database": "openregs", "table": "federal_register", "rows": [["2017-24163", "Medical Devices; Exemptions From Premarket Notification: Class II Devices; Request for Comments", "Notice", "The Food and Drug Administration (FDA or the Agency) is announcing its intent to exempt a list of class II devices from premarket notification requirements, subject to certain limitations. The Agency has determined that, based on established factors, these devices no longer require premarket notification to provide reasonable assurance of safety and effectiveness. FDA is publishing this notice to obtain comments regarding the proposed exemptions, in accordance with the Federal Food, Drug, and Cosmetic Act (the FD&C Act).", "2017-11-07", 2017, 11, "https://www.federalregister.gov/documents/2017/11/07/2017-24163/medical-devices-exemptions-from-premarket-notification-class-ii-devices-request-for-comments", "https://www.govinfo.gov/content/pkg/FR-2017-11-07/pdf/2017-24163.pdf", "Health and Human Services Department; Food and Drug Administration", "221,199", "The Food and Drug Administration (FDA or the Agency) is announcing its intent to exempt a list of class II devices from premarket notification requirements, subject to certain limitations. The Agency has determined that, based on established factors,...", 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": ["2017-24163"], "units": {}, "query_ms": 18.44565593637526, "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"}