510(k) K823446 ยท DTB Permanent Pacemaker Electrode
PRODUCTS IMPLANTABLE PACING LEAD,TINED
| Applicant | Oscor, Inc., Palm Harbor FL, US |
| Decision | Substantially Equivalent, Dec 3, 1982 |
| Received | Nov 16, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823446
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.