510(k) K182914 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
MC3 Vascular Access Kit 21030
| Applicant | Mc3 Incorporated, Dexter MI, US |
| Decision | Substantially Equivalent, Oct 29, 2018 |
| Received | Oct 18, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182914
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.