510(k) K935922 ยท MKJ Automated External Defibrillators (Non-Wearable)
360 SLX ADVISORY DEFIBRILLATOR
| Applicant | Medical Research Laboratories, Inc., Buffalo Grove IL, US |
| Decision | Substantially Equivalent, Dec 22, 1994 |
| Received | Dec 13, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935922
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.