510(k) K905416 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
VESSEL DILATOR
| Applicant | The R Group, Gainesvilles FL, US |
| Decision | Substantially Equivalent, Mar 25, 1991 |
| Received | Dec 4, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K905416
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.