510(k) K991169 ยท DTB Permanent Pacemaker Electrode
SX 53/15-BP, MODEL 124 853, SX 60/15-BP, MODEL 124 854
| Applicant | Biotronik, Inc., Lake Oswego OR, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Jul 1, 1999 |
| Received | Apr 7, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991169
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.