510(k) K910608 ยท DTB Permanent Pacemaker Electrode
PERMANENT IMPLANTABLE FH ENDOCARDIAL LEADS W/TIP
| Applicant | Biotronik, GmbH & Co., Lake Oswego OR, US |
| Decision | Substantially Equivalent, Jul 30, 1991 |
| Received | Feb 12, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K910608
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.