E-Brik Visualization Assistant
Jul 2022
64d
Jdi Surgical, Inc.
1
Total
1
Cleared
0
Denied
Jdi Surgical, Inc. — FDA 510(k) Submissions
Jdi Surgical, Inc. has submitted 1 FDA 510(k) premarket notifications since 2022, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Anti Fog Solution And Accessories, Endoscopy . Use the specialty filter in the sidebar to narrow results.
1 devices