Medical Device Manufacturer · FR , Montreuil

Phakos

4 submissions · 4 cleared · Since 2017
4
Total
4
Cleared
0
Denied

Phakos — FDA 510(k) Submissions

Phakos has submitted 4 FDA 510(k) premarket notifications since 2017, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Unit, Cryophthalmic, Ac-powered, Lens, Contact, Polymethylmethacrylate, Diagnostic . Use the specialty filter in the sidebar to narrow results.

4 devices
1–4 of 4
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All4 Ophthalmic 4