510(k) K883750 ยท DXY Implantable Pacemaker Pulse-Generator
VENTRALITH I
| Applicant | Bio Pace Technology, Inc., Butler PA, US |
| Decision | Substantially Equivalent, Jan 13, 1989 |
| Received | Sep 1, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883750
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.