Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K912555 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| GammaMed 12i radionuclide applicator systems, distributed by Varian Medical Systems, Palo Alto, CA | 2 | 01/11/2007 | Varian Medical Systems |
| GammaMed software program, version 5.07, vers. 5.08, vers.-usa, vers.-tst and vers.-row , part numbe... | 2 | 08/10/2006 | Varian Medical Systems |
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