510(k) K810494 ยท DTB Permanent Pacemaker Electrode
TYPE FH ENDOCARDIAL LEAD
| Applicant | Biotronik Sales, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 7, 1981 |
| Received | Feb 24, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810494
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.