Medical Device Recalls
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1 result found
510(K) Number: K050869 |
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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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Radiance Data Management System, Software Version 2.60, modification for the ABL800 Flex Blood Gas A... | 2 | 10/28/2006 | Radiometer America Inc |
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