510(k) K890988 ยท LDF Electrode, Pacemaker, Temporary
MODEL 3110 HEART WIRE & 3110P PEDIATRIC HEART WIRE
| Applicant | Pace Medical, Waltham MA, US |
| Decision | Substantially Equivalent, Aug 25, 1989 |
| Received | Feb 27, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890988
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.