Medical Device Recalls
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1 result found
510(K) Number: K936180 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Video Monitor Suspensions that may be on the following Fluoroscopic and Radiographic X-Ray systems: ... | 2 | 01/21/2014 | GE Healthcare, LLC |
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