STERISEAL OPHTHALMIC CANNULA
Jan 1995
159d
Pharma-Plast, Ltd.
1
Total
1
Cleared
0
Denied
Pharma-Plast, Ltd. — FDA 510(k) Submissions
Pharma-Plast, Ltd. 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 Cannula, Ophthalmic . Use the specialty filter in the sidebar to narrow results.
1 devices