SKALPI 3200
May 1995
167d
Wiscco Development, Inc.
1
Total
1
Cleared
0
Denied
Wiscco Development, Inc. — FDA 510(k) Submissions
Wiscco Development, Inc. has submitted 1 FDA 510(k) premarket notifications since 1995, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Vibrator, Therapeutic . Use the specialty filter in the sidebar to narrow results.
1 devices