510(k) K852688 ยท DXY Implantable Pacemaker Pulse-Generator
MEDTRONICS MODELS 8320/8322/8329
| Applicant | Medtronic Vascular, Minneapolis MN, US |
| Decision | Substantially Equivalent, Nov 1, 1985 |
| Received | Jun 25, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852688
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.