Medical Device Manufacturer · US , Mchenry , IL

Hamilton Kent

1 submissions · 1 cleared · Since 1981

Total

Cleared

Denied

Hamilton Kent — FDA 510(k) Submissions

Hamilton Kent has submitted 1 FDA 510(k) premarket notifications since 1981, of which 1 received clearance as substantially equivalent to a predicate device.

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

1 devices

1–1 of 1

SORBOTHANE

K810228 · KNP Orthosis, Corrective Shoe · Physical Medicine

Feb 1981 14d

Hamilton Kent

Hamilton Kent — FDA 510(k) Submissions

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