510(k) K791732 ยท DTB Permanent Pacemaker Electrode
IMPLANTABLE ENDOCARDIAL SCREW-IN ELEC
| Applicant | Oscor, Inc., Palm Harbor FL, US |
| Decision | Substantially Equivalent, Sep 19, 1979 |
| Received | Sep 5, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K791732
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.