510(k) K830950 ยท DTB Permanent Pacemaker Electrode
VASCULAR PRODUCTS IMPLANTABLE PACING
| Applicant | Oscor, Inc., Palm Harbor FL, US |
| Decision | Substantially Equivalent, Apr 18, 1983 |
| Received | Mar 25, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830950
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.