510(k) K770881 ยท DXY Implantable Pacemaker Pulse-Generator
GENERATOR, PULSE, BIPOLAR 3608
| Applicant | Cardiac Pacemakers, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Jun 20, 1977 |
| Received | May 16, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K770881
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.