510(k) K870622 ยท MKJ Automated External Defibrillators (Non-Wearable)
HEART*AID 1000
| Applicant | Cardiac Resucitator Corp., Portland OR, US |
| Decision | Substantially Equivalent, Apr 10, 1987 |
| Received | Feb 12, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870622
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.