Medical Device Manufacturer · US , Broomall , PA

Keeler, Ltd.

4 submissions · 4 cleared · Since 2010
4
Total
4
Cleared
0
Denied

Keeler, Ltd. — FDA 510(k) Submissions

Keeler, Ltd. has submitted 4 FDA 510(k) premarket notifications since 2010, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Tonometer, Manual, Biomicroscope, Slit-lamp, Ac-powered, Unit, Cryophthalmic, Ac-powered . Use the specialty filter in the sidebar to narrow results.

4 devices
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All4 Ophthalmic 4