510(k) K810808 ยท DXY Implantable Pacemaker Pulse-Generator
CORATOMIC MODEL OVALITH-920
| Applicant | Coratomic, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, May 15, 1981 |
| Received | Mar 24, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810808
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.