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U.S. Department of Health and Human Services

Premarket Approval (PMA)
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1 to 10 of 34 Results
productcode MGB PMA Number p Decision Date From 1/1/2009 Decision Date To 1/1/2010
 
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Device
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PMA
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7F FISH-SP DEVICE MORRIS INNOVATIVE RESEARCH INC P050043 S002 07/24/2009
ANGIO-SEAL VASCULAR CLOSURE DEVICE TERUMO MEDICAL CORPORATION P930038 S057 04/08/2009
ANGIO-SEAL VASCULAR CLOSURE DEVICE TERUMO MEDICAL CORPORATION P930038 S060 12/03/2009
ANGIO-SEAL VASULAR CLOSURE DEVICE TERUMO MEDICAL CORPORATION P930038 S058 05/07/2009
D-STAT FLOWABLE HEMOSTAT Vascular Solutions, Inc. P990037 S029 12/02/2009
M5 MYNX VASCULAR CLOSURE DEVICE Cordis US Corporation P040044 S011 04/08/2009
MYNX VASCULAR CLOSURE DEVICE Cordis US Corporation P040044 S016 08/04/2009
MYNX VASCULAR CLOSURE DEVICE Cordis US Corporation P040044 S021 12/11/2009
MYNX VASCULAR CLOSURE DEVICE Cordis US Corporation P040044 S015 07/13/2009
MYNX VASCULAR CLOSURE DEVICE Cordis US Corporation P040044 S010 01/08/2009
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