510(k) K890794 ยท LDF Electrode, Pacemaker, Temporary
DAIG PACEL(TM) FLOW DIRECTED PACING CATHETER
| Applicant | Daig Corp., Minnetonka MN, US |
| Decision | Substantially Equivalent, Jun 20, 1989 |
| Received | Feb 17, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890794
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.