510(k) K770951 ยท DXY Implantable Pacemaker Pulse-Generator
CARDIAC PACERS W/NARROW PULSE WIDTH
| Applicant | Cordis Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jun 20, 1977 |
| Received | May 25, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K770951
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.