510(k) K770507 ยท DXY Implantable Pacemaker Pulse-Generator
PULSE GENERATOR, LITKICRON MODEL 3-70H
| Applicant | Medcor, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 7, 1977 |
| Received | Mar 17, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K770507
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.