510(k) K873474 ยท LDF Electrode, Pacemaker, Temporary
SUTURELESS TEMPORARY EPICARDIAL PACING LEAD
| Applicant | Symbion, Inc., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Oct 7, 1987 |
| Received | Aug 31, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873474
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.