Medical Device Recalls
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1 result found
510(K) Number: K091629 |
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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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Proteus 235 Product Usage: The Proton Therapy System - Proteus 235 (brand names: Proteus Plus an... | 2 | 01/08/2019 | Ion Beam Applications S.A. |
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