510(k) K955923 ยท MKJ Automated External Defibrillators (Non-Wearable)
MEDI-TRACE COMBINATION DEFIBRILLATION & ECG ELECTRODE FOR LAERDAL
| Applicant | Graphic Controls Corp., Buafflo NY, US |
| Decision | Substantially Equivalent, Oct 24, 1996 |
| Received | Dec 28, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955923
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.