510(k) K032421 ยท MKJ Automated External Defibrillators (Non-Wearable)
AMBU PEDIATRIC MULTI-FUNCTION DEFIBRILLATION ELECTRODE
| Applicant | Ambu, Inc., Linthicum MD, US |
| Decision | Substantially Equivalent, Feb 27, 2004 |
| Received | Aug 5, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032421
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.