Medical Device Manufacturer · US , Palm Harbor , FL

Sulzer Oscor, Inc. - FDA 510(k) Cleared Devices

2 submissions · 1 cleared · Since 1997

Total

Cleared

Denied

Sulzer Oscor, Inc. has 1 FDA 510(k) cleared medical devices. Based in Palm Harbor, US.

Historical record: 1 cleared submissions from 1997 to 1999. Primary specialty: Cardiovascular.

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

FDA 510(k) cleared devices by Sulzer Oscor, Inc.

2 devices

1-2 of 2