Medical Device Manufacturer · GB , England

Medifield , Ltd. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1988

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Medifield , Ltd. Anesthesiology ✕

1 devices

1-1 of 1

Cleared Mar 31, 1988

'HILT-WAY' RESUSCITATOR

Anesthesiology · 71d