Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K032996 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Elekta Synergy The Elekta Synergy System is intended to be used for radiation therapy treatment o... | 2 | 08/29/2011 | Elekta, Inc. |
| Elekta Synergy Intended to be used for radiation therapy treatment of malignant neoplastic diseas... | 2 | 04/27/2010 | Elekta, Inc. |
| Elekta SL Series/Precise Digital Accelerator. The product is used with radiation therapy treatmen... | 2 | 03/18/2010 | Elekta, Inc. |
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