510(k) K901709 ยท DTB Permanent Pacemaker Electrode
DNP 60-B UNIPOLAR ENDOCARDIAL LEAD
| Applicant | Biotronik, GmbH & Co., Lake Oswego OR, US |
| Decision | Substantially Equivalent, May 22, 1990 |
| Received | Apr 13, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901709
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.