510(k) K913158 ยท DTB Permanent Pacemaker Electrode
MODIFIED OSCOR PY PACING LEADS/MODIFICATION
| Applicant | Oscor Medical Corp., Palm Harbor FL, US |
| Decision | Substantially Equivalent, Sep 23, 1991 |
| Received | Jul 8, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913158
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.