Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K232032 |
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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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| Brand Name: Hitachi Proton Beam Therapy System Ref: PROBEAT-FR | 2 | 02/20/2026 |
FEI # 1000162206 Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha |
| Brand Name: PROBEAT Product Name: PROBEAT-CR Model/Catalog Number: N/A Software Version: N/A Pro... | 2 | 09/12/2024 |
FEI # 3003993895 Hitachi America, Ltd., Particle Therapy Division |
| Brand Name: PROBEAT Product Name: PROBEAT-V Model/Catalog Number: N/A Software Version: N/A Prod... | 2 | 09/12/2024 |
FEI # 3003993895 Hitachi America, Ltd., Particle Therapy Division |
| Brand Name: PROBEAT Product Name: PROBEAT-FR Model/Catalog Number: N/A Software Version: N/A Pro... | 2 | 09/12/2024 |
FEI # 3003993895 Hitachi America, Ltd., Particle Therapy Division |
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