510(k) K810677 ยท DXY Implantable Pacemaker Pulse-Generator
MODELS 5976/5977 PACEMAKER PULSE GENER
| Applicant | Medtronic, Inc., Mounds View MN, US |
| Decision | Substantially Equivalent, May 27, 1981 |
| Received | Mar 13, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810677
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.