510(k) K872724 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
SHEATH/DILATORS
| Applicant | Med-West, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Sep 15, 1987 |
| Received | Jul 8, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K872724
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.