510(k) K181237 ยท DYB Introducer, Catheter
Glidesheath Slender Tibial Pedal Kit
| Applicant | Terumo Medical Corporation, Elkton MD, US |
| Decision | Substantially Equivalent, Aug 3, 2018 |
| Received | May 10, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181237
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.