FDA 510(k) Applications Submitted by FUJIFILM Healthcare Corporation
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K220295 | 02/02/2022 | ARIETTA 50 | FUJIFILM Healthcare Corporation |
| K221619 | 06/03/2022 | ECHELON Oval V6.2 MRI System | Fujifilm Healthcare Corporation |
| K223426 | 11/14/2022 | ECHELON Synergy MRI system | FUJIFILM Healthcare Corporation |
| K213829 | 12/08/2021 | SCENARIA View | FUJIFILM Healthcare Corporation |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact