Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K984328 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Elekta Leksell Gamma Knife C 1.2, 4 and 4C Product Usage: Leksell Gamma Knife is a teletherapy... | 2 | 11/30/2011 | Elekta, Inc. |
| Leksell Gamma Knife C | 2 | 04/29/2010 | Elekta, Inc. |
| Leksell Gamma Knife C | 2 | 04/22/2010 | Elekta, Inc. |
| Leksell Gamma Knife. Leksell Gamma Knife is a teletherapy device indicated for use in the stereot... | 2 | 04/13/2010 | Elekta, Inc. |
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