Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K100777 |
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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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The ABL software version 6.12 for the ABL800 and ABL700 analyzer. The analyzers are intended for the... | 2 | 08/08/2012 | Radiometer America Inc |
The ABL software version 6.12 for the ABL800 analyzer. The analyzers are intended for the in Vitro t... | 2 | 08/08/2012 | Radiometer America Inc |
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