510(k) K102972 ยท MKJ Automated External Defibrillators (Non-Wearable)
LIFEPAK 12
| Applicant | Physio-Control, Inc., Redmond WA, US |
| Decision | Substantially Equivalent, Dec 22, 2010 |
| Received | Oct 6, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K102972
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jan 16, 2017 | Physio-Control, Inc. LIFEPAK 12 Defibrillator/Monitor with End-Tidal CO2 option.
The device is used in various areas of the hospital such as critical areas (emergency departments, critical care, operating room, etc.) an Terminated |
MKJ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.