Medical Device Manufacturer · US , Bothell , WA

Verathon Incorporated - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2007

Total

Cleared

Denied

Verathon Incorporated has 5 FDA 510(k) cleared medical devices. Based in Bothell, US.

Historical record: 5 cleared submissions from 2007 to 2017. Primary specialty: Radiology.

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

FDA 510(k) Regulatory Record - Verathon Incorporated

5 devices

1-5 of 5