Vista Ophthalmics Vitrectomy Probe
May 2022
119d
Vista Ophthalmics, LLC
1
Total
1
Cleared
0
Denied
Vista Ophthalmics, LLC — FDA 510(k) Submissions
Vista Ophthalmics, LLC has submitted 1 FDA 510(k) premarket notifications since 2022, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Vitrectomy, Instrument Cutter . Use the specialty filter in the sidebar to narrow results.
1 devices