510(k) K855139 ยท LDF Electrode, Pacemaker, Temporary
FLEXON TEMPORARY CARDIAC CONDUCTIVE MULTIFILAMENT
| Applicant | Davis & Geck, Inc., Danbury CT, US |
| Decision | Substantially Equivalent, Feb 26, 1986 |
| Received | Dec 23, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K855139
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.