510(k) K230871 ยท OWB Interventional Fluoroscopic X-Ray System
EXTRON 5; EXTRON 7
| Applicant | DRTECH Corporation, Seongnam-Si, KR |
| Decision | Substantially Equivalent, Aug 17, 2023 |
| Received | Mar 30, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K230871
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.