Medical Device Manufacturer · US , Mchenry , IL

Antibodies, Inc. - FDA 510(k) Cleared Devices

16 submissions · 16 cleared · Since 1977

Total

Cleared

Denied

Antibodies, Inc. has 16 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 16 cleared submissions from 1977 to 1989. Primary specialty: Immunology.

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

Antibodies, 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 - Antibodies, Inc.

16 devices

1-12 of 16

CRITHIDNA ANTI-DNA TEST KIT

NEPHELRATE ANTISERUMS C3C

K781653 · CZW

Immunology · 42d

Cleared Nov 08, 1978

NEPHELRATE ANTIPERUMS LGM

K781654 · CFN

Immunology · 42d

Cleared Nov 08, 1978

NEPHELRATE ANTISERUMS 1GA

K781655 · CFN

Immunology · 42d

Cleared Nov 08, 1978

NEPHELRATE ANTISERUMS, IGG

K781656 · CFN

Immunology · 42d

Antibodies, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Antibodies, Inc.

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