Medical Device Manufacturer · US , Memphis , TN

Retina Tester

1 submissions · 1 cleared · Since 1992
1
Total
1
Cleared
0
Denied

Retina Tester — FDA 510(k) Submissions

Retina Tester has submitted 1 FDA 510(k) premarket notifications since 1992, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Photostimulator, Ac-powered . Use the specialty filter in the sidebar to narrow results.

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