Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K051602 |
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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 Luminos TF, AXIOM Iconos R100, AXIOM Iconos R200 and AXIOM Luminos dRF | 2 | 01/20/2023 | Siemens Medical Solutions USA, Inc |
AXIOM SIRESKOP SD, SIRESKOP SX, AXIOM LUMINOS System, X-Ray, Fluoroscopic, image-intensified; solid... | 2 | 02/23/2011 | Siemens Medical Solutions USA, Inc |
SIEMENS AXIOM Luminos TF and Sireskop SD Solid State x-ray imager (flat panel/digital imager), Fluor... | 2 | 08/13/2010 | Siemens Medical Solutions USA, Inc |
AXIOM Sireskop SD Model numbers 8890415 and 8890407. The product is intended for use as radiographi... | 2 | 05/06/2009 | Siemens Medical Solutions USA, Inc |
AXIOM Luminos TF, model number 10093902 Intended to be used for procedures that involve high skin... | 2 | 10/10/2008 | Siemens Medical Solutions USA, Inc |
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