510(k) K761143 ยท DXY Implantable Pacemaker Pulse-Generator
LITHIUM IODIDE BATTERY PACEMAKER (#201)
| Applicant | Pacesetter Systems, Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 23, 1976 |
| Received | Nov 26, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K761143
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.