510(k) K023099 ยท DTB Permanent Pacemaker Electrode
AROX 45-JBP; AROX 53-JBP; MEROX 45-JBP; MEROX 53-JBP
| Applicant | Biotronik, Inc., Lake Oswego OR, US |
| Decision | Substantially Equivalent, Oct 18, 2002 |
| Received | Sep 18, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K023099
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.