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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 10 of 23 Results
ProductCode: DQY Applicant: CORDIS CORP. Decision Date To: 11/30/2021
 
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510(K)
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adroit guiding catheter CORDIS CORP., A JOHNSON & JOHNSON CO. K131225 05/29/2013
modification to envoy and vista brite tip CORDIS CORP. K021593 06/13/2002
cordis m3 pta dilatation catheter CORDIS CORP. K003920 06/15/2001
cordis slalom pta balloon catheter CORDIS CORP. K003159 10/30/2000
cordis introducer guide CORDIS CORP. K001136 04/28/2000
envoy and vista brite tip CORDIS CORP. K000715 03/31/2000
vista brite tip catheters CORDIS CORP. K992673 10/12/1999
6f envoy guiding catheter CORDIS CORP. K982770 08/18/1998
envoy and vista brite tip CORDIS CORP. K982632 08/18/1998
vista brite tip guiding catheters CORDIS CORP. K972978 10/21/1997
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