510(k) K914555 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
WORKSTATION FEMORAL INTRAVASCULAR RETRIEVAL (MODI)
| Applicant | Med Institute, Inc., West Lafayette IN, US |
| Decision | Substantially Equivalent, Jan 3, 1992 |
| Received | Oct 7, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914555
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.