510(k) K023205 ยท DTB Permanent Pacemaker Electrode
ELOX P 45-BP; ELOX P 53-BP; ELOX P 60-BP
| Applicant | Biotronik, Inc., Lake Oswego OR, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Apr 24, 2003 |
| Received | Sep 25, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023205
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.