510(k) K863879 ยท DXY Implantable Pacemaker Pulse-Generator
NEOS-M VS-1 PULSE GENERATOR
| Applicant | Biotronik Sales, Inc., Lake Oswego OR, US |
| Decision | Substantially Equivalent, Dec 10, 1986 |
| Received | Oct 6, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863879
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.