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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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