Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K042404 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
LIFEPAK 1000 defibrillator. Affected Part Numbers: 320371500XXX The LP1000 (in AED mode) is indi... | 2 | 05/23/2014 | Physio-Control, Inc. |
LIFEPAK 1000 defibrillator - portable battery powered semi-automated model that can be operated in e... | 2 | 09/16/2008 | Physio Control, Inc. |
-