510(k) K041883 ยท MKJ Automated External Defibrillators (Non-Wearable)
SKINTACT MULTIFUNCTION ELECTRODES, MODEL DF 21
| Applicant | Leonhard Lang GmbH, Stillwater MN, US |
| Decision | Substantially Equivalent, Sep 7, 2004 |
| Received | Jul 12, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041883
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.