This page includes the latest FDA filings for Cordis Corp A Johnson Johnson Co. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Device Company | Device | Date |
|---|---|---|
Cordis Corporation, A Johnson & Johnson Company | ELITECROSS Support Catheter | 2015-05-19 |
CORDIS CORPORATION, A JOHNSON & JOHNSON CO. | OUTBACK Elite Re-Entry Catheter | 2015-04-29 |
CORDIS CORP., A JOHNSON & JOHNSON CO. | MICRO GUIDE CATHETER ELITE | 2014-11-14 |
CORDIS CORP., A JOHNSON & JOHNSON CO. | ADROIT GUIDING CATHETER | 2013-05-29 |
CORDIS CORP., A JOHNSON & JOHNSON CO. | OPTEASE VENA CAVA FILTER AND RETRIEVAL CATHETER | 2010-02-04 |
CORDIS CORP., A JOHNSON & JOHNSON CO. | OUTBACK LTD RE-ENTRY CATHETER, MODEL: OTB42120 | 2009-01-13 |
CORDIS CORP., A JOHNSON & JOHNSON CO. | ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE AND ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE | 2006-09-22 |