510(k) K993139 ยท DTB Permanent Pacemaker Electrode
YP 45/15-BP; YP 53/15-BP; YP 60/15-BP
| Applicant | Biotronik, Inc., Lake Oswego OR, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Dec 17, 1999 |
| Received | Sep 20, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K993139
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.