VIVASCOPE SYSTEM, MODEL 1500, 3000
Sep 2008
181d
Lucid, Inc.
1
Total
1
Cleared
0
Denied
Lucid, Inc. — FDA 510(k) Submissions
Lucid, Inc. has submitted 1 FDA 510(k) premarket notifications since 2008, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Light Based Imaging . Use the specialty filter in the sidebar to narrow results.
1 devices