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Millipore Corporation

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K093815 LIGHT DIAGNOSTICS HUMAN METAPNEUMOVIRUS DFA KIT, MODEL CATALOG NUMBER 3124OMG2010-03-12 View
510(k) K081527 LIGHT DIAGNOSTICS HSV 1/2 TYPING DFA KITGQL2009-04-01 View
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