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U.S. Department of Health and Human Services

510(k) Premarket Notification
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11 to 17 of 17 Results
ProductCode: DYB Applicant: THOMAS MEDICAL PRODUCTS, INC Decision Date To: 10/27/2016
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510(K)
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modification to transseptal introducer set THOMAS MEDICAL PRODUCTS, INC. K020090 02/11/2002
modification to braided guiding introducer system THOMAS MEDICAL PRODUCTS, INC. K040713 06/01/2004
large bore splittable introducer kit THOMAS MEDICAL PRODUCTS, INC. K043438 02/15/2005
reinforced catheter introducer system (rcis) THOMAS MEDICAL PRODUCTS, INC. K081341 05/14/2008
crossover THOMAS MEDICAL PRODUCTS, INC. K083269 02/03/2009
coronary sinus guide and lateral vein introducer kits THOMAS MEDICAL PRODUCTS, INC. K120158 08/14/2012
heartspan steerable introducer kit THOMAS MEDICAL PRODUCTS, INC. K122431 01/29/2013
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