510(k) K896443 ยท DTB Permanent Pacemaker Electrode
MYOPORE(TM) UNIPOLAR MODELS 1117 & 1118 PACE LEADS
| Applicant | Possis Medical, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Dec 20, 1989 |
| Received | Nov 9, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896443
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.