Medical Device Recalls
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1 result found
510(K) Number: K130992 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| DS/US Proton Feature with Pinnacle3 Software Version 10.0.0 and 14.0.0 Radiation Therapy Planning S... | 2 | 02/02/2016 |
FEI # 1218950 Philips Medical Systems |
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