Vanquish Water Vapor Ablation Device
Nov 2025
118d
Francis Medical, Inc.
1
Total
1
Cleared
0
Denied
Francis Medical, Inc. — FDA 510(k) Submissions
Francis Medical, Inc. has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 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.
1 devices