Shanghai Glovmax Enterprise Co.,Ltd is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Shanghai Glovmax Enterprise Co.,Ltd - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Shanghai Glovmax Enterprise Co.,Ltd has 4 FDA 510(k) cleared medical devices. Based in Great Neck, US.
Historical record: 4 cleared submissions from 2000 to 2002. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Shanghai Glovmax Enterprise Co.,Ltd Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Shanghai Glovmax Enterprise Co.,Ltd
4 devices
Cleared
May 31, 2002
SHANGHAI GLOVMAX ENTERPRISE POWDERED BLUE NITRILE EXAMINATION GLOVES
General Hospital
64d
Cleared
May 16, 2002
SHANGHAI GLOVMAX ENTERPRISE POWDERFREE BLUE NITRILE EXAMINATION GLOVES
General Hospital
49d
Cleared
Jan 12, 2000
SHANGHAI GLOVMAX ENTERPRISE CO., LTD. PRE-POWDERED VINYL PATIENT EXAMINATION...
General Hospital
58d
Cleared
Jan 12, 2000
SHANGHAI GLOVMAX ENTERPRISE CO, LTD., POWDER-FREE VINYL PATIENT EXAMINATION...
General Hospital
58d