Hitachi , Ltd.
FDA 510(k) & PMA Approved Devices — 7 products
Total Devices7
Categories3
Latest FDA decision2020-07-13
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K201042 | PROBEAT-CR | LHN | 2020-07-13 | View |
| 510(k) | K191801 | PROBEAT-CR | LHN | 2019-09-13 | View |
| 510(k) | K172087 | SANGRAY | MOT | 2017-10-27 | View |
| 510(k) | K163505 | ARIETTA PRECISION | IYN | 2017-05-30 | View |
| 510(k) | K162902 | ARIETTA Prologue Diagnostic Ultrasound system and Transducers | IYN | 2016-12-15 | View |
| 510(k) | K162583 | ALOKA LISENDO 880 | IYN | 2016-11-17 | View |
| 510(k) | K161163 | PROBEAT-V Proton Beam Therapy System with X-ray Limiting Accessory | LHN | 2016-07-13 | View |
No matching devices.