{"database": "openregs", "table": "federal_register", "rows": [["2017-25065", "Medical Devices; Exemption From Premarket Notification: Over-the-Counter Denture Repair Kits", "Notice", "The Food and Drug Administration (FDA or Agency) is announcing that it has received a petition requesting exemption from the premarket notification requirements for over-the-counter (OTC) denture repair kits. These devices consist of material, such as a resin monomer system of powder and liquid glues, which is intended to be applied permanently to a denture to mend cracks or breaks. FDA is publishing this notice to obtain comments in accordance with procedures established by the Food and Drug Administration Modernization Act of 1997 (FDAMA).", "2017-11-20", 2017, 11, "https://www.federalregister.gov/documents/2017/11/20/2017-25065/medical-devices-exemption-from-premarket-notification-over-the-counter-denture-repair-kits", "https://www.govinfo.gov/content/pkg/FR-2017-11-20/pdf/2017-25065.pdf", "Health and Human Services Department; Food and Drug Administration", "221,199", "The Food and Drug Administration (FDA or Agency) is announcing that it has received a petition requesting exemption from the premarket notification requirements for over-the-counter (OTC) denture repair kits. These devices consist of material, such as...", 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": ["2017-25065"], "units": {}, "query_ms": 153.7218950688839, "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"}