510(k) K761237 ยท DXY Implantable Pacemaker Pulse-Generator
ELEC. CIR. PACE. MO. LI-2,LI-3,LI-4,LI-5
| Applicant | Arco Medical Products Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 21, 1976 |
| Received | Dec 13, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K761237
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.