510(k) K030260 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
GELBFISH FLEX VASCULAR DILATOR
| Applicant | Vascumetrix, LLC, Mesa AZ, US |
| Decision | Substantially Equivalent, Feb 20, 2003 |
| Received | Jan 24, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K030260
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.