510(k) K831771 ยท DXY Implantable Pacemaker Pulse-Generator
IMPLANTABLE PROGRAM. CARDIAC PULSE GEN
| Applicant | Telectronics, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 16, 1983 |
| Received | Jun 2, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831771
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.