510(k) K023507 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
MODIFICATION TO GELBFISH VASCULAR DILATORS
| Applicant | Vascumetrix, LLC, Mesa AZ, US |
| Decision | Substantially Equivalent, Nov 8, 2002 |
| Received | Oct 18, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K023507
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.