Safeskin Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Safeskin Corp. - FDA 510(k) Cleared Devices
24
Total
24
Cleared
0
Denied
Safeskin Corp. has 24 FDA 510(k) cleared general hospital devices. Based in Coral Gables, US.
Historical record: 24 cleared submissions from 1988 to 2000.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Safeskin Corp.
24 devices
Cleared
Mar 02, 2000
SAFESKIN PFE-XTRA POWDER-FREE LATEX EXAMINATION GLOVES, PROTEIN CONTENT 50...
General Hospital
164d
Cleared
Jan 18, 2000
SAFESKIN TACTYLON PF POWDER-FREE SURGEON'S GLOVES
General Hospital
46d
Cleared
Oct 27, 1999
SAFESKIN POLYMER-COATED NITRILE EXAMINATION GLOVES, POWDER-FREE SHIELDMASTER...
General Hospital
65d
Cleared
Sep 10, 1999
SHIELDMASTER POWDERED PURPLE NITRILE EXAMINATION GLOVES
General Hospital
71d
Cleared
Aug 30, 1999
SAFESKIN PURPLE POWDER-FREE NITRILE EXAMINATION GLOVES FOR USE WITH...
General Hospital
66d
Cleared
Aug 25, 1999
SAFESKIN STERILE PURPLE NITRILE EXAMINATION GLOVES
General Hospital
68d
Cleared
Jul 26, 1999
SAFESKIN SYNTHETIC BINYO POWDER-FREE POLYMER COATED EXAMINATION GLOVES...
General Hospital
46d
Cleared
May 21, 1999
POWDER-FREE LATEX SURGEON'S GLOVE SAFESKIN PFS PLUS CONTAINS 50MLGM OR LESS...
General Hospital
32d
Cleared
May 06, 1997
SAFESKIN POWDERED EXAMINATION GLOVE
General Hospital
56d
Cleared
Dec 19, 1996
SAFESKIN
General Hospital
199d
Cleared
Aug 28, 1995
SAFESKIN SUPRA
General Hospital
61d
Cleared
Aug 28, 1995
SAFESKIN SUPRA
General Hospital
60d