510(k) K992543 ยท MKJ Automated External Defibrillators (Non-Wearable)
HEARTSTREAM XLT DEFIBRILLATOR/MONITOR, AC CHARGER, DC CHARGER, DATA CARD, SINGLE BAY ADAPTER, DEFIBRILLATOR PADS CABLE
| Applicant | Hewlett-Packard Co., Seattle WA, US |
| Decision | Substantially Equivalent, May 18, 2000 |
| Received | Jul 30, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992543
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.