510(k) K852253 ยท DTD Pacemaker Lead Adaptor
329 CORDIS ENCOR PREVENOUS ARTRIAL & VENTRICULAR
| Applicant | Cordis Corp., Miami FL, US |
| Decision | Substantially Equivalent, Jul 29, 1985 |
| Received | May 24, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852253
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.