510(k) K781623 ยท DTB Permanent Pacemaker Electrode
PACING MODELS MUM 860, MUM 890
| Applicant | R.E. Brown Co., Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Dec 8, 1978 |
| Received | Sep 20, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781623
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.