Medical Device Manufacturer · US , Leesburg , FL

Microlife Systems AG - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1999

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Microlife Systems AG General Hospital ✕

1 devices

1-1 of 1

Cleared Feb 25, 1999

MICROLIFE IT2CA1

General Hospital · 37d