Medical Device Recalls
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1 result found
510(K) Number: K122644 |
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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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Artis zee and Artis zeego model Interventional fluoroscopic x-ray foot switch accessory; Model Num... | 2 | 02/23/2018 | Siemens Medical Solutions USA, Inc |
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