{"data":{"id":"us/21-cfr-230.2","jurisdiction":"us","citation":"21 CFR 230.2","heading":"Purpose.","body":"The purpose of this part is to establish an efficient process for the certification of designated medical gases and to establish an effective system for surveillance of such gases.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER C—DRUGS: GENERAL","PART 230—CERTIFICATION AND POSTMARKETING REPORTING FOR DESIGNATED MEDICAL GASES","Subpart A—General Provisions"],"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":"62758a29111f7c12a70205743a1873fef0322f73202863e236d89d87f68f1797","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-230.1","next":"us/21-cfr-230.3"},"notice":"GroundRules: Original legal text. Not legal advice."}