510(k) K171491 ยท DYB Introducer, Catheter
R2P Destination Slender Guiding Sheath
| Applicant | Terumo Medical Corporation, Elkton MD, US |
| Decision | Substantially Equivalent, Oct 5, 2017 |
| Received | May 22, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171491
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.