510(k) K801113 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
DILATOR, VESSEL, FOR PERC. CATHETER.
| Applicant | Alva Medical, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Jul 28, 1980 |
| Received | May 12, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801113
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.