Medical Device Manufacturer · US , Dayton , OH

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

2 submissions · 2 cleared · Since 1986

Total

Cleared

Denied

Versacor, Inc. has 2 FDA 510(k) cleared medical devices. Based in Dayton, US.

Historical record: 2 cleared submissions from 1986 to 1986. Primary specialty: Cardiovascular.

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

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

2 devices

1-2 of 2