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U.S. Department of Health and Human Services

510(k) Premarket Notification
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11 to 13 of 13 Results
ProductCode: DQY Applicant: GUIDANT CORP. Decision Date To: 04/25/2024
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Device Name
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510(K)
Number
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viking optima guiding catheter GUIDANT CORP. K001435 06/02/2000
5f guiding catheter GUIDANT CORP. K000598 03/24/2000
acs viking guiding catheter GUIDANT CORP. K972484 09/26/1997
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