A 510(k) is a [[Premarket notification]] in which a device manufacturer anounces to the FDA its intended introduction of a medical device.
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fda_public
created
Sat, 23 Jun 2012 14:07:09 GMT
creator
dirkjan
modified
Sat, 23 Jun 2012 14:07:09 GMT
modifier
dirkjan
tags
FDA
Term
creator
dirkjan