510(k) K902288 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
MODIFIED LIFEPAK 9 MONITOR/DEFIBRILLATOR
| Applicant | Physio-Control Corp., Redmond WA, US |
| Decision | Substantially Equivalent, Feb 25, 1991 |
| Received | May 22, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902288
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Aug 28, 2010 | Physio Control, Inc. External Sterilizable Paddles for use with the LIFEPAK 9, LIFEPAK 9P, LIFEPAK 12, and LIFEPAK 20/20e Defibrillator/Monitor. Terminated |
LDD | None listed |
| Aug 28, 2010 | Physio Control, Inc. Pediatric Paddles attachments used with LIFEPAK 9, LIFEPAK 9P, LIFEPAK 12 and LIFEPAK 20/20e Defibrillator/Monitors. Terminated |
LDD | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.