Medical Device Manufacturer · US , Los Angeles , CA

Jeanine Alcantara Intl. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 1989

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Jeanine Alcantara Intl. General Hospital ✕

1 devices

1-1 of 1

Cleared Apr 28, 1989

PATIENT EXAMINATION GLOVE (LATEX)

General Hospital · 30d