AL-3300
Sep 1994
209d
Hoya Corp. USA
1
Total
1
Cleared
0
Denied
Hoya Corp. USA — FDA 510(k) Submissions
Hoya Corp. USA has submitted 1 FDA 510(k) premarket notifications since 1994, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Instrument, Measuring, Lens, Ac-powered . Use the specialty filter in the sidebar to narrow results.
1 devices