510(k) K913027 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
VESSEL DILATOR
| Applicant | Deseret Medical, Inc., Sandy UT, US |
| Decision | Substantially Equivalent, Nov 27, 1991 |
| Received | Jul 9, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913027
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.