Medical Device Recalls
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1 result found
510(K) Number: K982696 |
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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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Interplant Radiation Treatment Planning System, Interplant Release 3.4.0 Used when planning and p... | 2 | 06/23/2011 | Computerized Medical Systems Inc |
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