Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K081722 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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(Siemens Rad Fluoro Uro Systems) Ysio, Luminos Agile, Luminos dRF, and Uroskop Omnia systems with s... | 2 | 11/26/2013 | Siemens Medical Solutions USA, Inc |
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