510(k) K022210 ยท MKJ Automated External Defibrillators (Non-Wearable)
MULTIFUNCTIONAL ELECTRODE MODELS 9640, 9650
| Applicant | Cardiac Science, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Oct 4, 2002 |
| Received | Jul 8, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022210
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.