510(k) K881837 ยท DXY Implantable Pacemaker Pulse-Generator
OPTIMA MPT SERIES III PACEMAKER, 5281D AND 5282D
| Applicant | Telectronics, Inc., Englewood CO, US |
| Decision | Substantially Equivalent, Jul 18, 1988 |
| Received | May 2, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881837
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.