{"data":{"id":"us/21-cfr-862.1085","jurisdiction":"us","citation":"21 CFR 862.1085","heading":"Angiotensin I and renin test system.","body":"(a) Identification. An angiotensin I and renin test system is a device intended to measure the level of angiotensin I generated by renin in plasma. Angiotensin I measurements are used in the diagnosis and treatment of certain types of hypertension.\n(b) Classification. Class II.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER H—MEDICAL DEVICES","PART 862—CLINICAL CHEMISTRY AND CLINICAL TOXICOLOGY DEVICES","Subpart B—Clinical Chemistry Test Systems"],"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":"5844fe99c7d4fa75449b17a369dc445da2605ff7ed2df4bcf215ee0d863e5472","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-862.1080","next":"us/21-cfr-862.1090"},"notice":"GroundRules: Original legal text. Not legal advice."}