510(k) K200284 ยท MUH System, X-Ray, Extraoral Source, Digital
R-Sensor, R-Sensor
| Applicant | Remedi Co., Ltd., Seoul, KR |
| Decision | Substantially Equivalent, Feb 28, 2020 |
| Received | Feb 5, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200284
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.