Medical Device Manufacturer · US , Mchenry , IL

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

4 submissions · 4 cleared · Since 1979

Total

Cleared

Denied

Vesta, Inc. has 4 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 4 cleared submissions from 1979 to 1983. Primary specialty: Anesthesiology.

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

FDA 510(k) Regulatory Record - Vesta, Inc.

4 devices

1-4 of 4