These regulations implement the FDA's criteria for and authority requiring manufacturers to:
# Register initially using form [[FDA 2891]] and update annually thereafter
# To list manufactured devices using form [[FDA 2892]] and to update this list annually.
This is the regulation that initiatiates FDA oversight
bag
fda_public
created
Sat, 23 Jun 2012 18:17:58 GMT
creator
dirkjan
modified
Sat, 23 Jun 2012 18:17:58 GMT
modifier
dirkjan
tags
CFR
FDA
creator
dirkjan