510(k) K874183 ยท DTB Permanent Pacemaker Electrode
ACTIFIX (R) BIPOLAR ENDOCARDIAL SCREW-IN LEAD
| Applicant | Daig Corp., Minnetonka MN, US |
| Decision | Substantially Equivalent, Jan 29, 1988 |
| Received | Oct 13, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K874183
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.