510(k) K780940 ยท DXY Implantable Pacemaker Pulse-Generator
GENERATOR, PULSE, MODEL 160B
| Applicant | Telectronics, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 27, 1978 |
| Received | Jun 8, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780940
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.