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U.S. Department of Health and Human Services

510(k) Premarket Notification
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11 to 20 of 28 Results
ProductCode: DQO Applicant: CORDIS CORP. Decision Date To: 05/03/2024
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Export all 28 Records to ExcelExport to Excel | Download Files | More About 510(k)
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510(K)
Number
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transit infusion catheter CORDIS CORP. K936260 05/31/1994
cordis 7 french thrulumen catheter CORDIS CORP. K922891 06/23/1993
nylex catheters CORDIS CORP. K930479 04/21/1993
cordis 6 french paragon angiographic catheter CORDIS CORP. K921310 09/17/1992
cordis angiographic doppler cather CORDIS CORP. K915498 04/17/1992
cordis 5.0 french super torque catheters CORDIS CORP. K915836 02/11/1992
cordis dual lumen pressure monitoring catheter CORDIS CORP. K914141 10/23/1991
cordis 5.2 french super torque plus cardio cath CORDIS CORP. K914007 10/18/1991
cordis 8 french 0.084 i.d. ptca guiding catheter CORDIS CORP. K911703 06/28/1991
diaventional catheter CORDIS CORP. K905297 02/01/1991
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