Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K100890 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Varian High Energy Linear Accelerator: Varian Medical Systems, Palo Alto, CA 94304 Indicated fo... | 2 | 02/08/2011 | Varian Medical Systems, Inc. Oncology Systems |
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