Cordis Corp., A Johnson & Johnson Co. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Cordis Corp., A Johnson & Johnson Co. Cardiovascular ✕
5 devices
Cleared
Nov 14, 2014
MICRO GUIDE CATHETER ELITE
Cardiovascular
266d
Cleared
May 29, 2013
ADROIT GUIDING CATHETER
Cardiovascular
29d
Cleared
Feb 04, 2010
OPTEASE VENA CAVA FILTER AND RETRIEVAL CATHETER
Cardiovascular
296d
Cleared
Jan 13, 2009
OUTBACK LTD RE-ENTRY CATHETER, MODEL: OTB42120
Cardiovascular
22d
Cleared
Sep 22, 2006
ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE AND ANGIOGUARD RX EMBOLI CAPTURE...
Cardiovascular
24d