510(k) K173799 ยท DQY Catheter, Percutaneous
NaviCross 0.018
| Applicant | Terumo Corporation, Shibuya-Ku, JP |
| Decision | Substantially Equivalent, Mar 29, 2018 |
| Received | Dec 14, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173799
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.