510(k) K873158 ยท DXY Implantable Pacemaker Pulse-Generator
MODIFIED MULTICOR AND OMNI-STANICOR PACEMAKERS
| Applicant | Tpl-Cordis, Inc., Suffield CT, US |
| Decision | Substantially Equivalent, Jan 7, 1988 |
| Received | Aug 10, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873158
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.