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.

• 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.

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

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