510(k) K772026 ยท DXY Implantable Pacemaker Pulse-Generator
CARDIAC PULSE GENERATOR, MODEL 150L
| Applicant | Telectronics, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Nov 3, 1977 |
| Received | Oct 27, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K772026
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.