510(k) K990483 ยท DTB Permanent Pacemaker Electrode
RETROX RX 45-JBP 124774, 53-JBP 124775, 53-BP 124776, 60-124777
| Applicant | Biotronik, Inc., Lake Oswego OR, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Jun 3, 1999 |
| Received | Feb 16, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990483
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.