510(k) K883344 ยท MKJ Automated External Defibrillators (Non-Wearable)
HEARTSTART 1000S
| Applicant | Laerdal Mfg. Corp., Portland OR, US |
| Decision | Substantially Equivalent, Sep 12, 1988 |
| Received | Aug 9, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883344
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.