Catheter Connections, Inc. is one of 5098 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Catheter Connections, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Catheter Connections, Inc. has 7 FDA 510(k) cleared medical devices. Based in Park City, US.
Historical record: 7 cleared submissions from 2010 to 2015. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Catheter Connections, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Catheter Connections, Inc.
7 devices
Cleared
May 22, 2015
DualCap
General Hospital
235d
Cleared
Nov 19, 2014
DualCap IV Pole Strips(Disinfectant Caps for Male Luers)
General Hospital
84d
Cleared
Jan 22, 2013
CATHETER CONNECTIONS' DARK BLUE DUALCAP FOR MALE LUERS
General Hospital
27d
Cleared
Dec 14, 2012
CATHETER CONNECTIONS DUALCAP SOLO
General Hospital
74d
Cleared
Jan 27, 2012
CATHETER CONNECTIONS' DUALCAP SOLO
General Hospital
30d
Cleared
Nov 09, 2011
CATHETER CONNECTIONS' DUALCAP DUO
General Hospital
34d
Cleared
Apr 08, 2010
CATHETER CONNECTIONS DUALCAP
General Hospital
176d