510(k) K823253 ยท DXT Injector And Syringe, Angiographic
VERTEX MONITORING CATHETER
| Applicant | Vertex Medical Corp., Walker MI, US |
| Decision | Substantially Equivalent, Dec 30, 1982 |
| Received | Nov 1, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823253
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.