Medical Device Manufacturer · US , Blairstown , NJ

Clark Laboratories, Inc. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1992

Total

Cleared

Denied

Clark Laboratories, Inc. has 14 FDA 510(k) cleared medical devices. Based in Blairstown, US.

Historical record: 14 cleared submissions from 1992 to 1998. Primary specialty: Immunology.

Browse the FDA 510(k) cleared devices submitted by Clark Laboratories, Inc. Filter by specialty or product code using the sidebar.

Clark Laboratories, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Clark Laboratories, Inc.

14 devices

1-12 of 14

Cleared Jul 22, 1998

VCA IGM ELISA TEST SYSTEM

K980596 · LSE

Microbiology · 155d

Cleared Jul 22, 1998

VCA IGG ELISA TEST SYSTEM

K980912 · LSE

Microbiology · 134d

Cleared May 01, 1998

EBNA-1 IGM ELISA TEST SYSTEM

K980598 · LLM

Microbiology · 73d

Cleared Mar 26, 1998

EA-D IGG ELISA TEST SYSTEM

K973123 · LSE

Microbiology · 218d

Cleared Sep 08, 1993

ENCORE ENA COMBINED EIA

K931543 · LLL

Immunology · 163d

Cleared Jan 26, 1993

ENCORE THYROGLOBULIN IGE, IGA AND IGM EIA

ENCORE RHEUMATOID FACTOR EIA

K924056 · DHR

Immunology · 44d

Clark Laboratories, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Clark Laboratories, Inc.

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