510(k) K955722 ยท LDF Electrode, Pacemaker, Temporary
FLEXON TEMPORARY CARDIAC PACER LEAD
| Applicant | Davis & Geck, Inc., Danbury CT, US |
| Decision | Substantially Equivalent, Mar 15, 1996 |
| Received | Dec 18, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955722
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.