510(k) K780781 ยท DXY Implantable Pacemaker Pulse-Generator
STILITH CARDIAC PACEMAKERS-M. 60 & 120
| Applicant | R.E. Brown Co., Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 27, 1978 |
| Received | May 12, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780781
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.