510(k) K820939 ยท DXY Implantable Pacemaker Pulse-Generator
C-101-P
| Applicant | Coratomic, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 22, 1982 |
| Received | Apr 6, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820939
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.