{"data":{"id":"us/21-cfr-890.1600","jurisdiction":"us","citation":"21 CFR 890.1600","heading":"Intermittent pressure measurement system.","body":"(a) Identification. An intermittent pressure measurement system is an evaluative device intended for medical purposes, such as to measure the actual pressure between the body surface and the supporting media.\n(b) Classification. Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in § 890.9.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER H—MEDICAL DEVICES","PART 890—PHYSICAL MEDICINE DEVICES","Subpart B—Physical Medicine Diagnostic Devices"],"source_url":"https://www.ecfr.gov/api/versioner/v1/full/2026-08-25/title-21.xml","current_through":"2026-08-25","vintage":"","retrieved_at":"2026-08-27T02:24:47Z","sha256":"6c1f8b7ba847256b658dc8cc947c48b2892602cbab315c3c3364d7ce1e99cd4e","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-890.1575","next":"us/21-cfr-890.1615"},"notice":"GroundRules: Original legal text. Not legal advice."}