510(k) K193125 ยท DYB Introducer, Catheter
R2P Destination Slender Guiding Sheath
| Applicant | Terumo Medical Corporation, Elkton MD, US |
| Decision | Substantially Equivalent, Jan 6, 2020 |
| Received | Nov 12, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K193125
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.