510(k) K033681 ยท DYB Introducer, Catheter
GLIDESHEATH
| Applicant | Terumo Corp., Elkton MD, US |
| Decision | Substantially Equivalent, Dec 11, 2003 |
| Received | Nov 24, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K033681
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.