Cox Sterile Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cox Sterile Products, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Cox Sterile Products, Inc. has 4 FDA 510(k) cleared medical devices. Based in Dallas, US.
Historical record: 4 cleared submissions from 1987 to 1994. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Cox Sterile Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cox Sterile Products, Inc.
4 devices
Cleared
Sep 26, 1994
STERIKING, SEE & PEEL
General Hospital
857d
Cleared
May 08, 1992
DISINFECTION WITH THE COX DRY HEAT STERILIZER
General Hospital
430d
Cleared
Apr 13, 1988
COX RAPID HEAT TRANSFER STERILIZER W/12 MIN. CYCLE
General Hospital
12d
Cleared
Oct 29, 1987
COX RAPID HEAT TRANSFER STERILIZER
General Hospital
115d