Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K951358 |
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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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AXIOM SIRESKOP SD, SIRESKOP SX, AXIOM LUMINOS System, X-Ray, Fluoroscopic, image-intensified; solid... | 2 | 02/23/2011 | Siemens Medical Solutions USA, Inc |
AXIOM Sireskop SX Model numbers 3111676 and 3111668. The product is intended for use as radiographic... | 2 | 05/06/2009 | Siemens Medical Solutions USA, Inc |
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