{"data":{"id":"us/21-cfr-814.120","jurisdiction":"us","citation":"21 CFR 814.120","heading":"Temporary suspension of approval of an HDE.","body":"An HDE or HDE supplement may be temporarily suspended for the same reasons and in the same manner as prescribed for PMA's in § 814.47.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER H—MEDICAL DEVICES","PART 814—PREMARKET APPROVAL OF MEDICAL DEVICES","Subpart H—Humanitarian Use 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":"d611dbd2ac4ab1cbc5a98ba05831f4db431599798d65047b9f7763139c5b6208","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-814.118","next":"us/21-cfr-814.122"},"notice":"GroundRules: Original legal text. Not legal advice."}