Medical Device Manufacturer · US , West Chester , PA

Eye-Ko, Inc.

1 submissions · 1 cleared · Since 1986

Total

Cleared

Denied

Eye-Ko, Inc. — FDA 510(k) Submissions

Eye-Ko, Inc. has submitted 1 FDA 510(k) premarket notifications since 1986, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Hook, Ophthalmic . Use the specialty filter in the sidebar to narrow results.

1 devices

1–1 of 1

DISPOSAL SURGICAL INSTRUMENTS FOR OPHTHALMOLOGY

K864292 · HNQ Hook, Ophthalmic · Ophthalmic

Dec 1986 59d

Eye-Ko, Inc.

Eye-Ko, Inc. — FDA 510(k) Submissions

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