510(k) K831190 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
VESSEL DILATOR
| Applicant | Medrad, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, May 9, 1983 |
| Received | Apr 12, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831190
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.