Medical Device Recalls
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1 result found
510(K) Number: K063093 |
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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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Philips EasyVision MM workstation with software R10.2 and R11.1 The EasyVision MM Workstation is in... | 2 | 11/18/2010 | Philips Medical Systems North America Co. Phillips |
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