510(k) K172985 ยท FHN Ligator, Hemorrhoidal
Ligation Device
| Applicant | Leo Medical Co., Ltd., Changzhou, CN |
| Decision | Substantially Equivalent, Jun 14, 2018 |
| Received | Sep 27, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172985
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.