Medical Device Recalls
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1 result found
510(K) Number: K910902 |
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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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VMX, VMX Plus Mobile Radiographic Unit with the following models: 45296139; 45296200; 45296350; 45... | 2 | 04/10/2013 | GE Healthcare, LLC |
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