Company ยท US
Cordis Corp., A Johnson & Johnson Co.
FDA 510(k) clearances and medical device recalls filed under this name, 1999 to 2015. Name variants (Inc, Corp, punctuation) are merged.
11510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| May 19, 2015 | K150187 | ELITECROSS Support Catheter Cordis Corporation, A Johnson & Johnson Company | PDU |
| Apr 29, 2015 | K150836 | OUTBACK Elite Re-Entry Catheter Cordis Corporation, A Johnson & Johnson Co. | PDU |
| Nov 14, 2014 | K140438 | MICRO GUIDE CATHETER ELITE Cordis Corp., A Johnson & Johnson Co. | PDU |
| Mar 7, 2014 | K140286 | OPTEASE VENA CAVA FILTER AND OPTEASE RETRIEVAL CATHTETER Cordis, A Johnson & Johnson Co. | DTK |
| May 29, 2013 | K131225 | ADROIT GUIDING CATHETER Cordis Corp., A Johnson & Johnson Co. | DQY |
| Feb 4, 2010 | K091077 | OPTEASE VENA CAVA FILTER AND RETRIEVAL CATHETER Cordis Corp., A Johnson & Johnson Co. | DTK |
| Jan 13, 2009 | K083814 | OUTBACK LTD RE-ENTRY CATHETER, MODEL: OTB42120 Cordis Corp., A Johnson & Johnson Co. | PDU |
| Sep 22, 2006 | K062531 | ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE AND ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE Cordis Corp., A Johnson & Johnson Co. | NTE |
| Nov 28, 2001 | K013581 | CORDIS AVIATOR PERIPHERAL DILATATION CATHETER Cordis, A Johnson & Johnson Co. | DQY |
| Aug 1, 2001 | K012090 | CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT Cordis, A Johnson & Johnson Co. | FGE |
| Sep 15, 1999 | K992755 | CORDIS PALMAZ CORINTHIAN TRANSHEPATIC BILIARY STENT AND DELIVERY SYSTEM, CORDIS CRIMPING TOOLS, CORDIS INTRODUCER TUBE Cordis, A Johnson & Johnson Co. | FGE |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||