510(k) K760443 ยท DTB Permanent Pacemaker Electrode
CARDIAC ELECTRODE
| Applicant | Meadox Medicals, Div. Boston Scientific Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 26, 1976 |
| Received | Aug 16, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K760443
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.