Sunmax Enterprise Shanghai Co. , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sunmax Enterprise Shanghai Co. , Ltd. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Sunmax Enterprise Shanghai Co. , Ltd. has 5 FDA 510(k) cleared medical devices. Based in Great Neck, US.
Historical record: 5 cleared submissions from 1996 to 2009. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Sunmax Enterprise Shanghai Co. , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sunmax Enterprise Shanghai Co. , Ltd.
5 devices
Cleared
Jul 01, 2009
SUNMAX ENTERPRISE SHANGHAI CO. POWDER FREE BLUE NITRILE PATIENT EXAMINATION...
General Hospital
141d
Cleared
Aug 16, 2001
SUNMAX BLUE NITRILE POWDER-FREE EXAMINATION GLOVE
General Hospital
70d
Cleared
Aug 14, 2001
SUNMAX BLUE NITRILE POWDERED EXAMINATION GLOVES
General Hospital
71d
Cleared
Feb 07, 1997
POWDER-FREE VINYL PATIENT EXAMINATION GLOVES
General Hospital
58d
Cleared
Jun 27, 1996
SUNMAX ENTERPRISE SHANGHAI VINYL POWDERED PATIENT EXAM. GLOVES
General Hospital
125d