510(k) K172099 ยท DYB Introducer, Catheter
Shoocin Introducer Kit
| Applicant | Lepu Medical Technology (Beijing) Co., Ltd., Beijing, CN |
| Decision | Substantially Equivalent, Oct 5, 2017 |
| Received | Jul 11, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172099
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.