PHOENIX LASER SYSTEMS OPHTHALMIC SURGICAL WORKSTA.
Dec 1990
252d
Phoenix Laser Systems, Inc.
1
Total
1
Cleared
0
Denied
Phoenix Laser Systems, Inc. — FDA 510(k) Submissions
Phoenix Laser Systems, Inc. has submitted 1 FDA 510(k) premarket notifications since 1990, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Laser, Neodymium:yag, Ophthalmic For Posterior Capsulotomy And Cutting Pupilla . Use the specialty filter in the sidebar to narrow results.
1 devices