510(k) K945511 ยท MPE Auxiliary Power Supply (Acor Dc) For External Transcutaneous Cardiac Pacemaker
LIFEPAK 10 DEFIBRILLATOR/MONITOR/PACEMAKER, AND LIFEPAK 11 CARDIAC MONITOR
| Applicant | Physio-Control Corp., Redmond WA, US |
| Decision | Substantially Equivalent, Sep 26, 1995 |
| Received | Nov 9, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K945511
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.