510(k) K800352 ยท DTB Permanent Pacemaker Electrode
PACEMAKER, ELECTRODE
| Applicant | Daig Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, May 28, 1980 |
| Received | Feb 15, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800352
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.