Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K101508 |
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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-Proton Therapy System | 2 | 07/28/2021 | Ion Beam Applications S.A. |
Proteus 235, ProteusPLUS or Proteus ONE produces and delivers a proton beam for the treatment of pat... | 2 | 10/11/2018 | Ion Beam Applications S.A. |
Proteus 235, Version PTS-11.0.1.2 and PTS-11.0.2 Product Usage: A device designed to produce and... | 2 | 06/20/2018 | Ion Beam Applications S.A. |
Proteus 235, Proton Therapy System a medical device designed to produce and delivers a proton beam f... | 2 | 03/09/2018 | Ion Beam Applications S.A. |
Proteus 235, graphite block 8 | 2 | 03/08/2018 | Ion Beam Applications S.A. |
Proteus 235 | 2 | 03/23/2017 | Ion Beam Applications S.A. |
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