IN-VITRO DIAGNOSTIC VAGINITIS TEST KIT
Sep 2005
202d
Ameritek Research, LLC
1
Total
1
Cleared
0
Denied
Ameritek Research, LLC — FDA 510(k) Submissions
Ameritek Research, LLC has submitted 1 FDA 510(k) premarket notifications since 2005, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Discs, Strips And Reagents, Microorganism Differentiation . Use the specialty filter in the sidebar to narrow results.
1 devices