510(k) K860466 ยท DXY Implantable Pacemaker Pulse-Generator
MODEL 329D, SERIERS R BIOPOLAR CARDIAC PUL. GEN.
| Applicant | Cook Pacemaker Corp., Leechburg PA, US |
| Decision | Substantially Equivalent, Feb 24, 1986 |
| Received | Feb 6, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860466
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.