510(k) K964107 ยท DTB Permanent Pacemaker Electrode
OSCOR PERMANENT RETRACTABLE SCREW-IN PACING LEAD MODEL PR
| Applicant | Oscor Medical Corp., Palm Harbor FL, US |
| Decision | Substantially Equivalent - Subject to Tracking & PMS, Apr 1, 1997 |
| Received | Oct 15, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964107
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.