510(k) K844969 ยท DTC Analyzer, Pacemaker Generator Function
CORDIS DUAL-CHAMBER PSA MODEL 296A (PACEMAKER)
| Applicant | Cordis Corp., Miami FL, US |
| Decision | Substantially Equivalent, May 1, 1985 |
| Received | Dec 24, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K844969
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.