510(k) K905300 ยท DTB Permanent Pacemaker Electrode
PERMANENT PACING LEAD
| Applicant | Oscor Medical Corp., Palm Harbor FL, US |
| Decision | Substantially Equivalent, May 7, 1991 |
| Received | Nov 27, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K905300
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.