PUMA-G System
Apr 2019
159d
Coaptech, LLC
1
Total
1
Cleared
0
Denied
Coaptech, LLC — FDA 510(k) Submissions
Coaptech, LLC has submitted 1 FDA 510(k) premarket notifications since 2019, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Tube, Gastro-enterostomy . Use the specialty filter in the sidebar to narrow results.
1 devices