510(k) K954609 ยท MKJ Automated External Defibrillators (Non-Wearable)
HEARTSTART 911
| Applicant | Laerdal Medical Corp., Wappingers Falls NY, US |
| Decision | Substantially Equivalent, Jan 4, 1996 |
| Received | Oct 4, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954609
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.