Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha
Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha holds FDA 510(k) medical device clearances, first cleared 2022, most recent 2024, with 2 FDA device recalls on record.
Top product codes for Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha
FDA recalls by Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha
- Z-1429-2026 — Brand Name: Hitachi Proton Beam Therapy System Ref: PROBEAT-FR
- Z-1430-2026 — Brand Name: Hitachi Proton Beam Therapy REF: PROBEAT-CR
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha
Data sourced from openFDA. This site is unofficial and independent of the FDA.