510(k) K801763 ยท DXY Implantable Pacemaker Pulse-Generator
VIVALITH 5, - MDL-201A & TDL-201A
| Applicant | Pacesetter Systems, Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 27, 1980 |
| Received | Jul 28, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801763
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.