510(k) K220295 ยท IYN System, Imaging, Pulsed Doppler, Ultrasonic
ARIETTA 50
| Applicant | Fujifilm Healthcare Corporation, Kashiwa-Shi, JP |
| Decision | Substantially Equivalent, Apr 29, 2022 |
| Received | Feb 2, 2022 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K220295
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.