510(k) K021217 ยท DTB Permanent Pacemaker Electrode
AROX 53-BP; AROX 60-BP; AROX 45-JBP; AROX 53-JBP
| Applicant | Biotronik, Inc., Lake Oswego OR, US |
| Decision | Substantially Equivalent, May 1, 2002 |
| Received | Apr 17, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K021217
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.