510(k) K893763 ยท DTB Permanent Pacemaker Electrode
MODELS 1113 AND 1114 PACEMAKER LEADS
| Applicant | Possis Medical, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Jul 14, 1989 |
| Received | May 19, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893763
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.