510(k) K882067 ยท MKJ Automated External Defibrillators (Non-Wearable)
MARQUETTE 1200 DEFIBRILLATOR
| Applicant | Marquette Electronics, Inc., Milwaukee WI, US |
| Decision | Substantially Equivalent, Nov 17, 1988 |
| Received | May 17, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882067
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.