510(k) K852748 ยท DXY Implantable Pacemaker Pulse-Generator
CORDIS MODELS 336A,336B,337A & 334 CARDIAC PACEMAK
| Applicant | Cordis Corp., Miami FL, US |
| Decision | Substantially Equivalent, Nov 1, 1985 |
| Received | Jun 27, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852748
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.