510(k) K000763 ยท DTB Permanent Pacemaker Electrode
PX 53/15-BP, MODEL 130 050 AND PX 60/15-BP, MODEL 130 051
| Applicant | Biotronik, GmbH & Co., Lake Oswego OR, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Apr 6, 2000 |
| Received | Mar 9, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K000763
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.