510(k) K012256 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
GELBISH VASCULAR DILATOR
| Applicant | Vascumetrix, LLC, Meas AZ, US |
| Decision | Substantially Equivalent, Dec 20, 2001 |
| Received | Jul 18, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012256
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.