Medical Device Recalls
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1 result found
510(K) Number: K093967 |
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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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Varian Treatment version 6.6.5052. Varian Medical Systems, Palo Alto, Ca Intended to provide a... | 2 | 08/31/2011 | Varian Medical Systems, Inc. Oncology Systems |
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