510(k) K822595 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
VESSEL DILATOR
| Applicant | Vertex Medical Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 28, 1982 |
| Received | Aug 27, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K822595
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.