Medical Device Manufacturer · US , Norwich , NY

Culture Kits, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1985

Total

Cleared

Denied

Culture Kits, Inc. has 9 FDA 510(k) cleared medical devices. Based in Norwich, US.

Historical record: 9 cleared submissions from 1985 to 1991. Primary specialty: Microbiology.

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

Culture Kits, 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 - Culture Kits, Inc.

9 devices

1-9 of 9

Cleared Oct 04, 1991

URI-THREE(TM), MODIFICATION

MUELLER HINTON SENSITIVITY PLATE

Culture Kits, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Culture Kits, Inc.

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