Medical Device Manufacturer · MY , Selangor

Mwe Asia America Industries Sdn - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1989

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Mwe Asia America Industries Sdn General Hospital ✕

1 devices

1-1 of 1

Cleared Aug 23, 1989

PATIENT EXAMINATION GLOVE (LATEX)

General Hospital · 145d