21 CFR Part 810
PART 810—MEDICAL DEVICE RECALL AUTHORITY
- PART 810—MEDICAL DEVICE RECALL AUTHORITY
- Chapter I—Food and Drug Administration, Department of Health and Human Services › Subchapter H—Medical Devices
- Subpart A—General Provisions
- § 810.1 Scope.
- § 810.2 Definitions.
- § 810.3 Computation of time.
- § 810.4 Service of orders.
- Subpart B—Mandatory Medical Device Recall Procedures
- § 810.10 Cease distribution and notification order.
- § 810.11 Regulatory hearing.
- § 810.12 Written request for review of cease distribution and notification order.
- § 810.13 Mandatory recall order.
- § 810.14 Cease distribution and notification or mandatory recall strategy.
- § 810.15 Communications concerning a cease distribution and notification or mandatory recall order.
- § 810.16 Cease distribution and notification or mandatory recall order status reports.
- § 810.17 Termination of a cease distribution and notification or mandatory recall order.
- § 810.18 Public notice.
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