Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K120197 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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ABL90 FLEX software version 2.7 MR3. The ABL90 FLEX analyzer is intended for in vitro testing of sa... | 2 | 08/08/2012 | Radiometer America Inc |
ABL90 FLEX analyzers with software versions 3.3MR1 or below. The ABL90 FLEX Analyzer is a portable, ... | 2 | 10/01/2018 | Radiometer America Inc |
ABL90 FLEX analyzer; Model number 393-090. A portable, automated analyzer that measures pH, blood g... | 2 | 02/09/2015 | Radiometer America Inc |
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