510(k) K041459 ยท MKJ Automated External Defibrillators (Non-Wearable)
LIFEPAK 12 DEFIBRILLATOR/MONITOR
| Applicant | Medtronic Emergency Response Systems, Inc., Redmond WA, US |
| Decision | Substantially Equivalent, Jul 1, 2004 |
| Received | Jun 2, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K041459
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.