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The Electronic Code of Federal Regulations (e-CFR) is a regularly updated, unofficial editorial compilation of CFR material and Federal Register amendments produced by the National Archives and Records Administration's Office of the Federal Register (OFR) and the Government Printing Office.

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Electronic Code of Federal Regulations

blue pill

e-CFR Data is current as of September 17, 2014

Title 21Chapter ISubchapter HPart 810


TITLE 21—Food and Drugs

CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)

SUBCHAPTER H—MEDICAL DEVICES

PART 810—MEDICAL DEVICE RECALL AUTHORITY

rule

Subpart A—GENERAL PROVISIONS

§810.1
Scope.
§810.2
Definitions.
§810.3
Computation of time.
§810.4
Service of orders.
rule

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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