Medical Device Manufacturer · US , Plymouth , MN

Venturemed Group, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2020

Total

Cleared

Denied

Venturemed Group, Inc. has 1 FDA 510(k) cleared medical devices. Based in Plymouth, US.

Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Cardiovascular.

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

FDA 510(k) cleared devices by Venturemed Group, Inc.

1 devices

1-1 of 1