Medical Device Manufacturer · US , Baltimore , MD

Coaptech, Inc.

2 submissions · 2 cleared · Since 2023
2
Total
2
Cleared
0
Denied

Coaptech, Inc. — FDA 510(k) Submissions

Coaptech, Inc. has submitted 2 FDA 510(k) premarket notifications since 2023, of which 2 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.

2 devices
1–2 of 2
Filters
Filter by Specialty
All2 Gastroenterology & Urology 2