510(k) K942440 ยท DTB Permanent Pacemaker Electrode
AFP CARDIAC PACING SYSTEM MODEL 283
| Applicant | Siemens-Pacesetter, Inc., Sylmar CA, US |
| Decision | Substantially Equivalent - Subject to Tracking Reg., Aug 8, 1994 |
| Received | May 20, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K942440
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.