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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 10 of 28 Results
ProductCode: DQO Applicant: CORDIS CORP. Decision Date To: 05/03/2024
 
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510(K)
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steri-sleeve CORDIS CORP. K802629 10/31/1980
ptca guiding cather CORDIS CORP. K844161 01/02/1985
modified cordis ptca guiding catheters CORDIS CORP. K854576 02/26/1986
cordis contrast injection lines CORDIS CORP. K864141 11/03/1986
modifications to cordis' super flow catheters CORDIS CORP. K862244 08/25/1986
stand & high flow femoral-ventricular pigtail cath CORDIS CORP. K862006 06/27/1986
double lumen catheter CORDIS CORP. K872248 08/12/1987
cordis shuttle catheter CORDIS CORP. K896308 03/28/1990
diaventional catheter CORDIS CORP. K905297 02/01/1991
cordis 5.0 french super torque catheters CORDIS CORP. K915836 02/11/1992
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