Medical Device Manufacturer · US , Mchenry , IL

Calbiochem-Behring Corp. - FDA 510(k) Cleared Devices

41 submissions · 41 cleared · Since 1978

Total

Cleared

Denied

Calbiochem-Behring Corp. has 41 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 41 cleared submissions from 1978 to 1983. Primary specialty: Immunology.

Browse the FDA 510(k) cleared devices submitted by Calbiochem-Behring Corp. Filter by specialty or product code using the sidebar.

Calbiochem-Behring Corp. 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 - Calbiochem-Behring Corp.

41 devices

1-12 of 41

Cleared Jul 28, 1983

REVOLUTION RADIAL IMMUNODIFFUSION PLATE

K831811 · JZQ

Immunology · 52d

Cleared Apr 27, 1983

ENA TEST KIT SM & RNP AUTO ANTIBODY

CREATINE KINASE-MB KIT

K820812 · JHY

Toxicology · 20d

Cleared Mar 04, 1982

ENZYGNOST TM RUBELLA IGM

K813493 · LFX

Immunology · 80d

Cleared Jan 26, 1982

AFT SYSTEM PROFICIENCY TESTING PROGRAM

RUBELLA ANTIBODIES TEST REAGENTS

K810309 · GOL

Immunology · 34d

Cleared Mar 11, 1981

RHEUMATOID FACTORS REFERENCE SERUM

K810404 · DHR

Microbiology · 21d

Cleared Dec 18, 1980

RUBELLA ELISA REAGENTS RUBELLA IGG ANTI

K802102 · GOL

Immunology · 106d

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Calbiochem-Behring Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Calbiochem-Behring Corp.

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