Medical Device Manufacturer · US , Walker , MI

Institute Virion , Ltd. - FDA 510(k) Cleared Devices

16 submissions · 16 cleared · Since 1984

Total

Cleared

Denied

Institute Virion , Ltd. has 16 FDA 510(k) cleared microbiology devices. Based in Walker, US.

Historical record: 16 cleared submissions from 1984 to 1986.

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

Institute Virion , Ltd. 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 - Institute Virion , Ltd.

16 devices

1-12 of 16

Cleared Sep 30, 1986

COMPLEMENT-FIXATION TEST FOR CAMPYLOBACTER JEJUNI

MEASLES VIRUS RUBEOLA

RESPIRATORY SYNCYTIAL VIRUS

K843673 · GQG

Microbiology · 374d

Cleared Sep 26, 1985

VARICELLA/ZOSTER VIRUS

Institute Virion , Ltd. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Institute Virion , Ltd.

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