Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K151856 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| AQURE System Software Version 2.2.0 Model #: 933-599 UDI: (01)05700699335999(10)2.2.0 Catalog ... | 2 | 12/22/2016 |
FEI # 3010420736 Radiometer America Inc |
| AQURE System; Model Number: 933-599. The AQURE System manages blood gas and immunoassay analyzers. | 2 | 02/03/2016 |
FEI # 3010420736 Radiometer America Inc |
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