510(k) K180473 ยท OWB Interventional Fluoroscopic X-Ray System
ANYVIEW DR SERIES FPD Fluoroscopic Mobile C-arm ANYVIEW-240DR, ANYVIEW-320DR, ANYVIEW-500DR
| Applicant | Ecotron Co., Ltd., Seoul, KR |
| Decision | Substantially Equivalent, Mar 23, 2018 |
| Received | Feb 22, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K180473
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.