510(k) K902469 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
BYRD DILATOR SHEATH SET - TEFLON
| Applicant | Medical Engineering and Development Institute, West Lafayette IN, US |
| Decision | Substantially Equivalent, Aug 23, 1990 |
| Received | Jun 4, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902469
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.