510(k) K790344 ยท DTB Permanent Pacemaker Electrode
BIPOLAR PERNENOUS VENTRICULAR LEAD
| Applicant | Cordis Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 17, 1979 |
| Received | Feb 21, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790344
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.