Medical Device Manufacturer · US , Hillsborough , NC

Interlogics, Inc.

1 submissions · 1 cleared · Since 1997

Total

Cleared

Denied

Interlogics, Inc. — FDA 510(k) Submissions

Interlogics, Inc. has submitted 1 FDA 510(k) premarket notifications since 1997, of which 1 received clearance as substantially equivalent to a predicate device.

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

1 devices

1–1 of 1

INTERLOGICS W-TRACKER AND WRIST WORKS SOFTWARE

K971079 · KQX Goniometer, Ac-powered · Neurology

Jul 1997 106d

Interlogics, Inc.

Interlogics, Inc. — FDA 510(k) Submissions

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