Medical Device Manufacturer · US , Queen'S Village , NY

H.B.M. USA Co.,Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2005

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - H.B.M. USA Co.,Inc. General Hospital ✕

1 devices

1-1 of 1

Cleared May 11, 2005

MEDISPO (POWDERED) AND MEDISPO-PF (POWDER-FREE) SURGEONS GLOVE

General Hospital · 119d