510(k)
Revision as of 07:18, 25 August 2020 by Dirkjan (talk | contribs) (Created page with "A 510(k) is a Premarket notification in which a device manufacturer anounces to the FDA its intended introduction of a medical device. Category:fd...")
A 510(k) is a Premarket notification in which a device manufacturer anounces to the FDA its intended introduction of a medical device.
