AIRGENT, MODEL AG7000010
Jan 2009
178d
Perfaction, Inc.
1
Total
1
Cleared
0
Denied
Perfaction, Inc. — FDA 510(k) Submissions
Perfaction, Inc. has submitted 1 FDA 510(k) premarket notifications since 2009, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Injector, Fluid, Non-electrically Powered . Use the specialty filter in the sidebar to narrow results.
1 devices