510(k) K914185 ยท LDF Electrode, Pacemaker, Temporary
PACEL(TM) FLOW DIRECTED PACING CATHETER
| Applicant | Daig Corp., Minnetonka MN, US |
| Decision | Substantially Equivalent, Jan 27, 1992 |
| Received | Sep 18, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914185
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.