Hitachi Healthcare Americas
FDA 510(k) & PMA Approved Devices — 12 products
Total Devices12
Categories4
Latest Approval2021-10-07
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K211406 | OASIS MRI System | LNH | 2021-10-07 | View |
| 510(k) | K202422 | Arietta 65 | IYN | 2020-11-04 | View |
| 510(k) | K202030 | OASIS MRI System | LNH | 2020-10-21 | View |
| 510(k) | K200498 | SCENARIA View | JAK | 2020-07-17 | View |
| 510(k) | K192851 | OASIS MRI System | LNH | 2020-02-21 | View |
| 510(k) | K190841 | SCENARIA View | JAK | 2019-09-13 | View |
| 510(k) | K191233 | ARIETTA 750 | IYN | 2019-08-09 | View |
| 510(k) | K190248 | ARIETTA 50 | IYN | 2019-04-02 | View |
| 510(k) | K183291 | Supria True64 Whole-Body X-Ray CT System | JAK | 2019-02-01 | View |
| 510(k) | K183456 | Aloka Arietta 850 | IYN | 2019-01-28 | View |
| 510(k) | K172492 | Optical Topography System ETG-4100 | DQA | 2018-08-17 | View |
| 510(k) | K180901 | Low Dose CT Lung Cancer Screening Option | JAK | 2018-05-16 | View |
No matching devices.