GroundRules
21 CFR 803.22: What are the circumstances in which I am not required to file a report?
Where this section sits in the code
- Title 21—Food and Drugs
- CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
- SUBCHAPTER H—MEDICAL DEVICES
- PART 803—MEDICAL DEVICE REPORTING
- Subpart B—Generally Applicable Requirements for Individual Adverse Event Reports
(a) If you become aware of information from multiple sources regarding the same patient and same reportable event, you may submit one medical device report.
(b) You are not required to submit a medical device report if:
(1) You are a user facility, importer, or manufacturer, and you determine that the information received is erroneous in that a device-related adverse event did not occur. You must retain documentation of these reports in your MDR files for the time periods specified in § 803.18.
(2) You are a manufacturer or importer and you did not manufacture or import the device about which you have adverse event information. When you receive reportable event information in error, you must forward this information to us with a cover letter explaining that you did not manufacture or import the device in question.
Collected 2026-08-27T02:24:47Z. Source file · JSON