510(k) K771262 ยท DXY Implantable Pacemaker Pulse-Generator
PACEMAKER & CARDIAC LEAD, BIPOLAR
| Applicant | Arco Medical Products Co., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 21, 1977 |
| Received | Jul 11, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K771262
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.