Medical Device Manufacturer · US , Totowa , NJ

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

3 submissions · 3 cleared · Since 2011

Total

Cleared

Denied

Vectracor, Inc. has 3 FDA 510(k) cleared medical devices. Based in Totowa, US.

Historical record: 3 cleared submissions from 2011 to 2018. Primary specialty: Cardiovascular.

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

Vectracor, Inc. is one of 5098 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

Vectracor, Inc. — FDA 510(k) Products and Clearance History

3 devices

1-3 of 3