Aqua Medical, Inc.

Aqua Medical, Inc. — FDA 510(k) Submissions

Aqua Medical, Inc. has submitted 5 FDA 510(k) premarket notifications since 2019, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Unit, Electrosurgical, Endoscopic (with Or Without Accessories) . Use the specialty filter in the sidebar to narrow results.