Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K043218 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Lactate Membrane units for E7077 Electrode Radiometer Medical ApS. The intended use is in vitro test... | 2 | 09/30/2013 |
FEI # 1523456 Radiometer America Inc |
| ABL800 FLEX Series analyzer with FLEXQ module-equipped with software version 5.2 to 5.27 | 2 | 04/06/2007 |
FEI # 1523456 Radiometer America Inc |
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