Medical Device Manufacturer · US , Woburn , MA

Genus Diagnostics - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1985

Total

Cleared

Denied

Genus Diagnostics has 9 FDA 510(k) cleared medical devices. Based in Woburn, US.

Historical record: 9 cleared submissions from 1985 to 1986. Primary specialty: Pathology.

Browse the FDA 510(k) cleared devices submitted by Genus Diagnostics Filter by specialty or product code using the sidebar.

Genus Diagnostics 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 - Genus Diagnostics

9 devices

1-9 of 9

RMK GENCELLS CULTURE SYSTEM

Genus Diagnostics - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Genus Diagnostics

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