510(k) K881356 ยท LDF Electrode, Pacemaker, Temporary
EXTERNAL PACEMAKER WIRE DRESSING CHANGE
| Applicant | Neal & Assoc., Inc., Columbia MO, US |
| Decision | Substantially Equivalent, May 19, 1988 |
| Received | Mar 28, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881356
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.