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The Code of Federal Regulations (CFR) annual edition is the codification of the general and permanent rules published in the Federal Register by the departments and agencies of the Federal Government produced by the Office of the Federal Register (OFR) and the Government Publishing Office.


Parallel Table of Authorities and Rules for the Code of Federal Regulations and the United States Code
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Electronic Code of Federal Regulations

Electronic Code of Federal Regulations

e-CFR data is current as of August 27, 2015

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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