{"database": "openregs", "table": "federal_register", "rows": [["2012-28042", "Medical Devices; Custom Devices; Request for Comments", "Notice", "The Food and Drug Administration Safety and Innovation Act (FDASIA), which was signed into law on July 9, 2012, amended the Federal Food, Drug, and Cosmetic Act (the FD&C Act). The Food and Drug Administration (FDA) is in the process of developing an implementation strategy and policy for the custom device exemption criteria in the FD&C Act amended by FDASIA. FDA is seeking information on appropriate uses of the custom device exemption.", "2012-11-19", 2012, 11, "https://www.federalregister.gov/documents/2012/11/19/2012-28042/medical-devices-custom-devices-request-for-comments", "https://www.govinfo.gov/content/pkg/FR-2012-11-19/pdf/2012-28042.pdf", "Health and Human Services Department; Food and Drug Administration", "221,199", "The Food and Drug Administration Safety and Innovation Act (FDASIA), which was signed into law on July 9, 2012, amended the Federal Food, Drug, and Cosmetic Act (the FD&C Act). The Food and Drug Administration (FDA) is in the process of developing an...", 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": ["2012-28042"], "units": {}, "query_ms": 0.3524511121213436, "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"}