510(k) K962467 ยท LDF Electrode, Pacemaker, Temporary
RV PACING LEAD
| Applicant | Abbott Laboratories, Abbott Park IL, US |
| Decision | Substantially Equivalent, Sep 17, 1996 |
| Received | Jun 25, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962467
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.