510(k) K896824 ยท DTB Permanent Pacemaker Electrode
BIOTRONIK'S PS-ENDOCARDIAL LEADS
| Applicant | Biotronik, GmbH & Co., Lake Oswego OR, US |
| Decision | Substantially Equivalent, Aug 8, 1990 |
| Received | Dec 4, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896824
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.