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U.S. Department of Health and Human Services

Premarket Approval (PMA)
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31 to 34 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
Number
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MYNX VASCULAR CLOSURE DEVICE Cordis US Corporation P040044 S012 04/15/2009
M5 MYNX VASCULAR CLOSURE DEVICE Cordis US Corporation P040044 S011 04/08/2009
ANGIO-SEAL VASCULAR CLOSURE DEVICE TERUMO MEDICAL CORPORATION P930038 S057 04/08/2009
MYNX VASCULAR CLOSURE DEVICE Cordis US Corporation P040044 S010 01/08/2009
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