Medical Device Manufacturer · US , Rapid City , SD

Sime Darby USA - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1989

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Sime Darby USA General Hospital ✕

2 devices

1-2 of 2

Cleared Sep 19, 1990

STERILE LATEX EXAMINATION GLOVES

General Hospital · 54d

Cleared Mar 24, 1989

PATIENT EXAMINATION GLOVES (LATEX)

General Hospital · 9d