510(k) K881153 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
LIFEPAK 9 DEFIBRILLATOR AND CARDIAC MONITOR
| Applicant | Physio-Control Corp., Redmond WA, US |
| Decision | Substantially Equivalent, Jul 27, 1988 |
| Received | Mar 17, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881153
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Apr 7, 2009 | Physio Control, Inc. Internal Sterilizable Paddles (electrodes) and Handles without discharge control for use with LIFEPAK 9 and LIFEPAK 9P defibrillators/monitors. Terminated |
LDD | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.