510(k) K122600 ยท MKJ Automated External Defibrillators (Non-Wearable)
LIFEPAK 1000 DEFIBRILLATOR
| Applicant | Physio-Control, Inc., Redmond WA, US |
| Decision | Substantially Equivalent, Oct 11, 2012 |
| Received | Aug 27, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K122600
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 3, 2017 | Physio-Control, Inc. The LIFEPAK 1000 defibrillator is intended for use by personnel who are authorized by a physician/medical director and are trained in CPR and the use of the LIFEPAK 1000 defibrillator. Terminated |
MKJ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.