{"database": "openregs", "table": "federal_register", "rows": [["2016-23633", "Medical Devices; Neurological Devices; Classification of the Evoked Photon Image Capture Device", "Rule", "The Food and Drug Administration (FDA) is classifying the Evoked Photon Image Capture Device into class I (general controls). The Agency is classifying the device into class I (general controls) in order to provide a reasonable assurance of safety and effectiveness of the device.", "2016-09-30", 2016, 9, "https://www.federalregister.gov/documents/2016/09/30/2016-23633/medical-devices-neurological-devices-classification-of-the-evoked-photon-image-capture-device", "https://www.govinfo.gov/content/pkg/FR-2016-09-30/pdf/2016-23633.pdf", "Health and Human Services Department; Food and Drug Administration", "221,199", "The Food and Drug Administration (FDA) is classifying the Evoked Photon Image Capture Device into class I (general controls). The Agency is classifying the device into class I (general controls) in order to provide a reasonable assurance of safety and...", 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": ["2016-23633"], "units": {}, "query_ms": 13.862299034371972, "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"}