510(k) K003072 ยท DTB Permanent Pacemaker Electrode
PACING LEADS, GUIDE WIRES, AND VARIOUS ACCESSORIES
| Applicant | Biotronik, Inc., Lake Oswego OR, US |
| Decision | Substantially Equivalent, Jan 9, 2001 |
| Received | Oct 3, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K003072
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.