Medical Device Recalls
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11 to 12 of 12 Results
510(K) Number: K120676 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
MEVION S250i, MEVION S250; Proton Radiation Treatment System | 2 | 06/22/2020 | Mevion Medical Systems, Inc. |
Mevion S250 and S250i Proton Therapy Systems hand pendant (P/N 10263 or P/N 37808) | 2 | 03/25/2022 | Mevion Medical Systems, Inc. |
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