510(k) K894240 ยท DXY Implantable Pacemaker Pulse-Generator
NEOS 02
| Applicant | Biotronik Cardiac Pacemakers, Lake Oswego CA, US |
| Decision | Substantially Equivalent, Oct 26, 1989 |
| Received | Jun 20, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894240
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.