Creative Care Systems, Inc. - FDA 510(k) Cleared Devices
7
Total
6
Cleared
0
Denied
Creative Care Systems, Inc. has 6 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 6 cleared submissions from 1984 to 1986. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Creative Care Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Creative Care Systems, Inc.
7 devices
Cleared
May 06, 1986
NON-KOR WINGED INFUSION SETS
General Hospital
21d
Cleared
Sep 19, 1985
NON-KOR ACCESS KITS
General Hospital
79d
Cleared
May 07, 1985
PERCUTANEOUS CV CATHETER INSERTION KIT W OR W/O CV
General Hospital
64d
Cleared
May 01, 1985
DRESSING CHANGE KIT
General Hospital
58d
Cleared
Jul 06, 1984
NON-CORING NEEDLE
General Hospital
70d
Cleared
Apr 17, 1984
DAYPAK SYS VII CATHETER CARE KIT
Anesthesiology
47d
Cleared
Apr 16, 1984
DAYPAK SYSTEM III CATHETER CARE KIT
General Hospital
61d