510(k) K841802 ยท LDF Electrode, Pacemaker, Temporary
ELECTRODE CATHETER, ORTHOGONAL TYPE
| Applicant | Webster Laboratories, Inc., Altadena CA, US |
| Decision | Substantially Equivalent, Oct 18, 1984 |
| Received | May 1, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K841802
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.