510(k) K874738 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
10 AND 12 FRENCH VESSEL DILATORS
| Applicant | Impra, Inc., Tempe AZ, US |
| Decision | Substantially Equivalent, May 2, 1988 |
| Received | Nov 18, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K874738
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.