Medical Device Manufacturer · US , Bloomfield Hills , MI

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

1 submissions · 1 cleared · Since 1997

Recent clearances: VERSATEC 310 ELECTRODE

1

Total

1

Cleared

0

Denied

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

1 devices

1-1 of 1

Cleared Jan 07, 1997

VERSATEC 310 ELECTRODE

Cardiovascular · 96d