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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K051804
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FDA Recall
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ABL80-FLEX-393-839 Box Label, REF 393-839, IVD, CE, UDI: 05700693938394 - Product Usage: It is inte... 2 06/29/2020 Radiometer Medical ApS
ABL80 FLEX (with FLEX software) and ABL80 FLEX CO-OX (with CO-OX software) - pH Blood Gas and Electr... 2 08/30/2012 Sendx Medical Inc
SenDx Medical Inc ABL80FLEX Blood Gas, pH, Electrolyte, and Metabolite System The ABL80 F... 2 04/09/2012 Sendx Medical Inc
ABL8O FLEX Software Version 1.10 included in the ABL8O Flex Analyzer, Model Number 914863 2 08/29/2007 Sendx Medical Inc
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