[Code of Federal Regulations]
[Title 21, Volume 8]
[Revised as of April 1, 2008]
From the U.S. Government Printing Office via GPO Access
[CITE: 21CFR822.28]

[Page 171]
 
                        TITLE 21--FOOD AND DRUGS
 
CHAPTER I--FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN 
                          SERVICES (CONTINUED)
 
PART 822_POSTMARKET SURVEILLANCE--Table of Contents
 
               Subpart E_Responsibilities of Manufacturers
 
Sec. 822.28  If I stop marketing the device subject to postmarket
surveillance, what must I do?

    You must continue to conduct postmarket surveillance in accordance 
with your approved plan even if you no longer market the device. You may 
request that we allow you to terminate postmarket surveillance or modify 
your postmarket surveillance because you no longer market the device. We 
will make these decisions on a case-by-case basis, and you must continue 
to conduct the postmarket surveillance unless we notify you that you may 
stop your surveillance study.

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