510(k) K885175 ยท DTB Permanent Pacemaker Electrode
MYOPORE(TM) UNIPOLAR SUTURELESS MYOCARDIAL LEADS
| Applicant | Possis Medical, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Jul 14, 1989 |
| Received | Dec 14, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K885175
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.