{"database": "openregs", "table": "cfr_sections", "rows": [["21:21:8.0.1.1.32.6.1.15", 21, "Food and Drugs", "I", "H", "890", "PART 890\u2014PHYSICAL MEDICINE DEVICES", "F", "Subpart F\u2014Physical Medicine Therapeutic Devices", "890.5360", "\u00a7 890.5360 Measuring exercise equipment.", "FDA", "21 U.S.C. 351, 360, 360c, 360e, 360j, 360 l, 371.", "48 FR 53047, Nov. 23, 1983, unless otherwise noted.", "[48 FR 53047, Nov. 23, 1983, as amended at 84 FR 71818, Dec. 30, 2019; 85 FR 44188, July 22, 2020]", "(a)  Identification.  Measuring exercise equipment consist of manual devices intended for medical purposes, such as to redevelop muscles or restore motion to joints or for use as an adjunct treatment for obesity. These devices also include instrumentation, such as the pulse rate monitor, that provide information used for physical evaluation and physical planning purposes., Examples include a therapeutic exercise bicycle with measuring instrumentation, a manually propelled treadmill with measuring instrumentation, and a rowing machine with measuring instrumentation.\n\n(b)  Classification.  Class II (special controls). The device, when it is a measuring exerciser or an interactive rehabilitation exercise device for prescription use only, is exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in \u00a7 890.9."]], "columns": ["section_id", "title_number", "title_name", "chapter", "subchapter", "part_number", "part_name", "subpart", "subpart_name", "section_number", "section_heading", "agency", "authority", "source_citation", "amendment_citations", "full_text"], "primary_keys": ["section_id"], "primary_key_values": ["21:21:8.0.1.1.32.6.1.15"], "units": {}, "query_ms": 0.24443899746984243, "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"}