Title 21

PART 810

Part 810 - Medical Device Recall Authority

PART 810 - MEDICAL DEVICE RECALL AUTHORITY Authority:21 U.S.C. 321, 331, 332, 333, 334, 351, 352, 355, 360h, 360i, 371, 374, 375. Source:61 FR 59018, Nov. 20, 1996, unless otherwise noted.

21:8.0.1.1.8.1SUBPART A
Subpart A - General Provisions
21:8.0.1.1.8.1.1.1SECTION 810.1
   810.1 Scope.
21:8.0.1.1.8.1.1.2SECTION 810.2
   810.2 Definitions.
21:8.0.1.1.8.1.1.3SECTION 810.3
   810.3 Computation of time.
21:8.0.1.1.8.1.1.4SECTION 810.4
   810.4 Service of orders.
21:8.0.1.1.8.2SUBPART B
Subpart B - Mandatory Medical Device Recall Procedures
21:8.0.1.1.8.2.1.1SECTION 810.10
   810.10 Cease distribution and notification order.
21:8.0.1.1.8.2.1.2SECTION 810.11
   810.11 Regulatory hearing.
21:8.0.1.1.8.2.1.3SECTION 810.12
   810.12 Written request for review of cease distribution and notification order.
21:8.0.1.1.8.2.1.4SECTION 810.13
   810.13 Mandatory recall order.
21:8.0.1.1.8.2.1.5SECTION 810.14
   810.14 Cease distribution and notification or mandatory recall strategy.
21:8.0.1.1.8.2.1.6SECTION 810.15
   810.15 Communications concerning a cease distribution and notification or mandatory recall order.
21:8.0.1.1.8.2.1.7SECTION 810.16
   810.16 Cease distribution and notification or mandatory recall order status reports.
21:8.0.1.1.8.2.1.8SECTION 810.17
   810.17 Termination of a cease distribution and notification or mandatory recall order.
21:8.0.1.1.8.2.1.9SECTION 810.18
   810.18 Public notice.