510(k) K771538 ยท DXY Implantable Pacemaker Pulse-Generator
LITHICRON MODEL 3-70C-B PULSE GENERATOR
| Applicant | Medcor, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 22, 1977 |
| Received | Aug 11, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K771538
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.