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U.S. Department of Health and Human Services

510(k) Premarket Notification
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1 to 10 of 13 Results
ProductCode: DQY Applicant: GUIDANT CORP. Decision Date To: 04/25/2024
 
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510(K)
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rapido cut-away cutter GUIDANT CORP. K031459 07/23/2003
agiltrac .035 peripheral dilatation catheter GUIDANT CORP. K023320 12/10/2002
agiltrac .035 peripheral dilatation catheter GUIDANT CORP. K022738 09/13/2002
rapido guiding catheter, 6f model# 6776; rapido guiding catheter, 8f model# 6775, 6777, 6778, 6779, 6780, 6781, 6782, GUIDANT CORP. K021455 08/02/2002
easytrak guiding catheter GUIDANT CORP. K021284 05/02/2002
agiltrac .018 peripheral dilatation catheter GUIDANT CORP. K020161 02/22/2002
modification to viking optima guiding catheter GUIDANT CORP. K013638 12/04/2001
viatrac 14 plus peripheral dilatation catheter GUIDANT CORP. K012050 09/06/2001
viking optima guiding catheter GUIDANT CORP. K012002 07/26/2001
aviator peripheral dilatation catheter GUIDANT CORP. K010831 06/13/2001
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