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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K232032
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Product Description
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Recall
Class
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FDA Recall
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Recalling Firm
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Brand Name: PROBEAT Product Name: PROBEAT-FR Model/Catalog Number: N/A Software Version: N/A Pro... 2 09/12/2024 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 Hitachi America, Ltd., Particle Therapy Division
Brand Name: PROBEAT Product Name: PROBEAT-CR Model/Catalog Number: N/A Software Version: N/A Pro... 2 09/12/2024 Hitachi America, Ltd., Particle Therapy Division
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