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U.S. Department of Health and Human Services

510(k) Premarket Notification
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11 to 20 of 23 Results
ProductCode: DQY Applicant: CORDIS CORP. Decision Date To: 11/30/2021
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Export all 23 Records to ExcelExport to Excel | Download Files | More About 510(k)
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510(K)
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cordis shuttle catheter CORDIS CORP. K915777 02/11/1992
cordis shuttle catheter w/ sideholes CORDIS CORP. K921311 09/09/1992
cordis slalom pta balloon catheter CORDIS CORP. K003159 10/30/2000
envoy and vista brite tip CORDIS CORP. K000715 03/31/2000
envoy and vista brite tip CORDIS CORP. K982632 08/18/1998
modification to envoy and vista brite tip CORDIS CORP. K021593 06/13/2002
modified ptca guiding catheters CORDIS CORP. K862975 09/23/1986
vista brite tip catheters CORDIS CORP. K962830 10/17/1996
vista brite tip catheters CORDIS CORP. K963962 05/07/1997
vista brite tip catheters CORDIS CORP. K965211 03/11/1997
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