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.

FDA 510(k) Regulatory Record - Genus Diagnostics

9 devices

1-9 of 9

RMK GENCELLS CULTURE SYSTEM

Genus Diagnostics - FDA 510(k) Cleared Devices

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