510(k) K954714 ยท DTB Permanent Pacemaker Electrode
AFP CARDIAC PACING SYSTEM MODEL 283 (MODIFICATION)
| Applicant | Pacesetter, Inc., Sylmar CA, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Feb 1, 1996 |
| Received | Oct 2, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954714
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.