Medical Device Manufacturer · US , Walker , MI

Meridia 12 Corp. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1983

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Meridia 12 Corp. Neurology ✕

1 devices

1-1 of 1

Cleared Oct 28, 1983

ELECTRONEURAL STIMULATOR 12

Neurology · 171d