Medical Device Manufacturer · US , Mchenry , IL

Flaitron Laboratories, Inc.

1 submissions · 1 cleared · Since 1983

Total

Cleared

Denied

Flaitron Laboratories, Inc. — FDA 510(k) Submissions

Flaitron Laboratories, Inc. has submitted 1 FDA 510(k) premarket notifications since 1983, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Methylene Blue, Tissue Stain . Use the specialty filter in the sidebar to narrow results.

1 devices

1–1 of 1

NEPHROLYTE

K831502 · KFC Methylene Blue, Tissue Stain · Pathology

Jul 1983 68d

Flaitron Laboratories, Inc.

Flaitron Laboratories, Inc. — FDA 510(k) Submissions

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