{"data":{"id":"us/21-cfr-822.6","jurisdiction":"us","citation":"21 CFR 822.6","heading":"When will you notify me that I am required to conduct postmarket surveillance?","body":"We will notify you as soon as we have determined that postmarket surveillance of your device is necessary, based on the identification of a surveillance question. This may occur during the review of a marketing application for your device, as your device goes to market, or after your device has been marketed for a period of time.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER H—MEDICAL DEVICES","PART 822—POSTMARKET SURVEILLANCE","Subpart B—Notification"],"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":"5d368f14126de7198308f0e7740e69f08fdb6829b2b9bf9d0d9c12d7fd8c9488","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-822.5","next":"us/21-cfr-822.7"},"notice":"GroundRules: Original legal text. Not legal advice."}