FDA 510(k) Applications Submitted by CORDIS CORP., A JOHNSON & JOHNSON CO.

FDA 510(k) Number Submission Date Device Name Applicant
K062531 08/29/2006 ANGIOGUARD XP EMBOLI CAPTURE GUIDEWIRE AND ANGIOGUARD RX EMBOLI CAPTURE GUIDEWIRE CORDIS CORP., A JOHNSON & JOHNSON CO.
K091077 04/14/2009 OPTEASE VENA CAVA FILTER AND RETRIEVAL CATHETER CORDIS CORP., A JOHNSON & JOHNSON CO.
K083814 12/22/2008 OUTBACK LTD RE-ENTRY CATHETER, MODEL: OTB42120 CORDIS CORP., A JOHNSON & JOHNSON CO.
K131225 04/30/2013 ADROIT GUIDING CATHETER CORDIS CORP., A JOHNSON & JOHNSON CO.
K140438 02/21/2014 MICRO GUIDE CATHETER ELITE CORDIS CORP., A JOHNSON & JOHNSON CO.


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