510(k) K952101 ยท MKJ Automated External Defibrillators (Non-Wearable)
MARQUETTE DEFIB ELECTRODES
| Applicant | Marquette Electronics, Inc., Jupiter FL, US |
| Decision | Substantially Equivalent, Sep 7, 1995 |
| Received | May 4, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952101
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.