510(k) K213223 ยท FHN Ligator, Hemorrhoidal
Multi-Band Ligator
| Applicant | Beijing Zksk Technology Co., Ltd., Beijing, CN |
| Decision | Substantially Equivalent, Jun 6, 2022 |
| Received | Sep 29, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213223
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.