Medical Device Manufacturer · US , Mchenry , IL

Litton Bionetics - FDA 510(k) Cleared Devices

15 submissions · 15 cleared · Since 1978

Total

Cleared

Denied

Litton Bionetics has 15 FDA 510(k) cleared microbiology devices. Based in Mchenry, US.

Historical record: 15 cleared submissions from 1978 to 1984.

Browse the complete list of FDA 510(k) cleared microbiology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Litton Bionetics 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 - Litton Bionetics

15 devices

1-12 of 15

ROTAVIRUS BIO-ENZABEAD SCREEN KIT

K834443 · LIQ

Immunology · 91d

Cleared Aug 08, 1983

CMV RQ BIO-ENZABEAD KIT

RUBELLA RQ BIO-ENZABEAD KIT

K821804 · LFX

Microbiology · 89d

Cleared Sep 16, 1980

TOXO BIO-BEAD TITRATION KIT

K801720 · GLZ

Microbiology · 55d

Cleared Sep 16, 1980

HSV BIO-BEAD TITRATION KIT

K801721 · GQN

Microbiology · 55d

Cleared Sep 16, 1980

CMV BIO-BEAD TITRATION KIT

K801722 · GQH

Microbiology · 55d

Cleared Jun 30, 1980

RUBELLA BIO-BEAD TITRATION KIT

K800789 · GOL

Microbiology · 83d

Cleared Nov 13, 1979

RUBELLA BIO-BEAD SCREEN KIT

K791610 · GOL

Microbiology · 84d

Cleared Nov 13, 1979

TOXO BIO-BEAD SCREEN KIT

K791611 · GLZ

Microbiology · 84d

Cleared Nov 13, 1979

CMV BIO-BEAD SCREEN KIT

K791612 · GQH

Microbiology · 84d

Litton Bionetics - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Litton Bionetics

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