510(k) K040775 ยท MKJ Automated External Defibrillators (Non-Wearable)
LIFEPAK 12
| Applicant | Medtronic Physio-Control Corp., Redmond WA, US |
| Decision | Substantially Equivalent, Apr 23, 2004 |
| Received | Mar 26, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K040775
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 3, 2005 | Medtronic Emergency Response Systems, Inc. LIFEPAK 12 defibrillator/ monitors biphasic Terminated |
MKJ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.