Medical Device Recalls
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1 result found
510(K) Number: K851031 |
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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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Ziehm Vista/Vista Plus C-Arm Interventional Fluoroscopic X-Ray System. Mobile Fluoroscopic Imagin... | 2 | 12/24/2013 | Ziehm Imaging Inc |
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