Medical Device Manufacturer · CA , Quebec

Genepoc, Inc. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2017

Total

Cleared

Denied

Genepoc, Inc. has 5 FDA 510(k) cleared medical devices. Based in Quebec, CA.

Historical record: 5 cleared submissions from 2017 to 2019. Primary specialty: Microbiology.

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

FDA 510(k) cleared devices by Genepoc, Inc.

5 devices

1-5 of 5