510(k) K172331 ยท DYB Introducer, Catheter
Type I, Type II, Type III, Type IV
| Applicant | Lepu Medical Technology (Beijing) Co., Ltd., Beijing, CN |
| Decision | Unknown, Mar 2, 2018 |
| Received | Aug 2, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172331
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.