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U.S. Department of Health and Human Services

510(k) Premarket Notification
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21 to 23 of 23 Results
ProductCode: DQY Applicant: CORDIS CORP. Decision Date To: 11/30/2021
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Device Name
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510(K)
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vista brite tip catheters CORDIS CORP. K971572 07/14/1997
vista brite tip catheters CORDIS CORP. K992673 10/12/1999
vista brite tip guiding catheters CORDIS CORP. K972978 10/21/1997
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