510(k) K833965 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
8 FRENCH DILATOR 15CM, W/LUER LOCK
| Applicant | Quinton, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 16, 1983 |
| Received | Nov 16, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K833965
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.