{"database": "openregs", "table": "federal_register", "rows": [["2014-15626", "Medical Devices; Physical Medicine Devices; Classification of the Nonpowered Lower Extremity Pressure Wrap", "Rule", "The Food and Drug Administration (FDA) is classifying the nonpowered lower extremity pressure wrap 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.", "2014-07-03", 2014, 7, "https://www.federalregister.gov/documents/2014/07/03/2014-15626/medical-devices-physical-medicine-devices-classification-of-the-nonpowered-lower-extremity-pressure", "https://www.govinfo.gov/content/pkg/FR-2014-07-03/pdf/2014-15626.pdf", "Health and Human Services Department; Food and Drug Administration", "221,199", "The Food and Drug Administration (FDA) is classifying the nonpowered lower extremity pressure wrap into class I (general controls). The Agency is classifying the device into class I (general controls) in order to provide a reasonable assurance of...", 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": ["2014-15626"], "units": {}, "query_ms": 216.30256006028503, "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"}