510(k) K842193 ยท DXY Implantable Pacemaker Pulse-Generator
MULTILITH PULSE GENERATORS, 1141 & 2141
| Applicant | Ela Medical, Inc., Minnetonka MN, US |
| Decision | Substantially Equivalent, Jan 10, 1985 |
| Received | Jun 4, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K842193
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.