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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: KRA Applicant: CORDIS NEUROVASCULAR, INC. Decision Date To: 05/17/2024
 
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modification to hypertransit infusion catheter CORDIS NEUROVASCULAR, INC. K070279 03/14/2007
hypertransit infusion catheter CORDIS NEUROVASCULAR, INC. K043538 04/18/2005
prowler select (10, 14, and plus) infusion catheters with and without pre-shaped tips CORDIS NEUROVASCULAR, INC. K021591 05/22/2002
prowler select 10 and 14 infusion catheters with and without pre-shaped tips CORDIS NEUROVASCULAR, INC. K020680 03/27/2002
prowler infusion catheters with pre-shaped tips CORDIS NEUROVASCULAR, INC. K003925 01/08/2001
prowler plus infusion catheter CORDIS NEUROVASCULAR, INC. K993266 10/28/1999
1 mass transit infusion catheter, 1 various CORDIS NEUROVASCULAR, INC. K983003 09/17/1998
ces masstransit infusion catheter CORDIS NEUROVASCULAR, INC. K974222 02/10/1998
transit/rapidtransit/speedster/prowler infusion catheter CORDIS NEUROVASCULAR, INC. K972518 11/04/1997
fg infusion catheter CORDIS NEUROVASCULAR, INC. K971306 07/14/1997
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