Medical Device Manufacturer · US , Minneapolis, , MN

Ortivus Us, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1998

Recent clearances: MOBIMED SYSTEM, (PEGASUS AND POLARIS)

View 1 510(k) Devices ↓

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Ortivus Us, Inc. Cardiovascular ✕

1 devices

1-1 of 1

Cleared Feb 19, 1998

MOBIMED SYSTEM, (PEGASUS AND POLARIS)

Cardiovascular · 168d