510(k) K782146 ยท DXY Implantable Pacemaker Pulse-Generator
PACEMAKER, MODEL DDP ELECTRONIC CIRCUIT
| Applicant | Arco Medical Products Co., Mchenry IL, US |
| Decision | Unknown, Dec 27, 1978 |
| Received | Dec 27, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K782146
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.