Medical Device Recalls
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1 result found
510(K) Number: K040896 |
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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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Siemens KinetDx 4.2 Workplace, Siemens Medical Solutions, Ann Arbor, MI; 10090235. Indicated for ... | 2 | 01/02/2009 | Siemens Medical Solutions, USA, Inc |
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