510(k) K974617 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
PERIPHERAL VASCULAR DILATOR
| Applicant | Endovascular Instruments, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Dec 1, 1998 |
| Received | Dec 11, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974617
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.