Shanghai Poseidon Plastic Products Co., Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Shanghai Poseidon Plastic Products Co., Ltd. - FDA 510(k) Cleared Dev...
8
Total
8
Cleared
0
Denied
Shanghai Poseidon Plastic Products Co., Ltd. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 8 cleared submissions from 1995 to 2000. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Shanghai Poseidon Plastic Products Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Shanghai Poseidon Plastic Products Co., Ltd.
8 devices
Cleared
Jul 26, 2000
NITRILE EXAMINATION GLOVES, PRE-POWDERED, COLOR WHITE
General Hospital
40d
Cleared
Jul 11, 2000
NITRILE EXAMINATION GLOVES, PRE-POWDERED, COLOR BLUE
General Hospital
25d
Cleared
Jun 12, 2000
MULTIPLE PRIVATE LABELS, NITRILE EXAM GLOVES, POWDER-FREE (WHITE)
General Hospital
25d
Cleared
May 23, 2000
NITRILE EXAM GLOVES, POWDER-FREE, COLOR BLUE
General Hospital
46d
Cleared
Feb 09, 2000
SHANGHAI POSEIDON POWDER-FREE SYNTHETIC VINYL EXAMINATION GLOVES, YELLOW
General Hospital
159d
Cleared
Dec 04, 1998
PRE-POWDERED NON-STERILE SYNTHETIC EXAMINATION GLOVE
General Hospital
109d
Cleared
Dec 30, 1996
POWDER FREE VINYL EXAMINATION GLOVE
General Hospital
47d
Cleared
Dec 11, 1995
SHANGHAI POSEDON PLASTIC PRODUCTS VINYL EXAM GLOVES
General Hospital
83d