510(k) K073089 ยท MKJ Automated External Defibrillators (Non-Wearable)
LIFEPAK 20E
| Applicant | Physio-Control, Inc., Redmond WA, US |
| Decision | Substantially Equivalent, Jul 29, 2008 |
| Received | Nov 1, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073089
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 18, 2011 | Physio Control, Inc. The LIFEPAK 20 defibrillator/monitor and LIFEPAK 20e. Product part numbers: 3202487-xxx, 3202488-000, U3202487-000, 3202488-015, and U3202488-000.
The LIFEPAK 20 defibrillator/monitor and LIFEPAK 20 Terminated |
MKJ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.