510(k) K926172 ยท MKJ Automated External Defibrillators (Non-Wearable)
SERIES 1500 DEFIBRILLATOR, MODIFICATION
| Applicant | Marquette Electronics, Inc., Milwaukee WI, US |
| Decision | Substantially Equivalent, Feb 25, 1993 |
| Received | Dec 1, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K926172
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.