510(k) K896919 ยท MKJ Automated External Defibrillators (Non-Wearable)
HEARTSTART 3000
| Applicant | Laerdal Medical Corp., Portland OR, US |
| Decision | Substantially Equivalent, May 3, 1990 |
| Received | Dec 12, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896919
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.