510(k) K061212 ยท DTB Permanent Pacemaker Electrode
BIOTRONIK ENDOCARDIAL PACING LEADS
| Applicant | Biotronik, Inc., Lake Oswego OR, US |
| Decision | Substantially Equivalent, Jul 10, 2006 |
| Received | May 1, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K061212
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.