510(k) K990338 ยท DXN System, Measurement, Blood-Pressure, Non-Invasive
NIBP AND CO2 OPTIONS FOR THE PHYSIO-CONTROL LIFEPAK 12 DEFIBRILLATOR/MONITOR SYSTEM
| Applicant | Physio-Control Corp., Redmond WA, US |
| Decision | Substantially Equivalent, Sep 1, 1999 |
| Received | Feb 3, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990338
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Feb 5, 2003 | Medtronic Physio Control Corp LIFEPAK 12 defibrillator/monitor is a portable, battery operated, complete acute cardiac care response system with both manual and semi-automatic defibrillation operation. It has the ability to exte Terminated |
MKJ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.