Medical Device Manufacturer · US , Chicago , IL

Coapt, LLC - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2017

Total

Cleared

Denied

Coapt, LLC has 3 FDA 510(k) cleared medical devices. Based in Chicago, US.

Historical record: 3 cleared submissions from 2017 to 2019. Primary specialty: Neurology.

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

FDA 510(k) cleared devices by Coapt, LLC

3 devices

1-3 of 3