Medical Device Manufacturer · US , Doylestown , PA

Neoforce Group, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2006

7

Total

7

Cleared

0

Denied

FDA 510(k) Regulatory Record - Neoforce Group, Inc. General Hospital ✕

1 devices

1-1 of 1

Cleared Jun 27, 2006

V-2200 INFANT INCUBATOR

General Hospital · 50d