510(k) K002079 ยท MKJ Automated External Defibrillators (Non-Wearable)
MULTI-FUNCTION DEFIBRILLATION ELECTRODE
| Applicant | Medicotest A/S, Washington DC, US |
| Decision | Substantially Equivalent, Feb 22, 2001 |
| Received | Jul 10, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002079
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.