510(k) K842220 ยท DXY Implantable Pacemaker Pulse-Generator
MULTILITH 2 PULSE GENERATOR 1141 & 2141
| Applicant | Ela Medical, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Nov 29, 1984 |
| Received | Jun 5, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K842220
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.