Medical Device Recalls
-
1 to 3 of 3 Results
510(K) Number: K991910 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Physio-Control LIFEPAK® 12 defibrillator/monitor. The LIFEPAK12 defibrillator/monitor series is a b... | 2 | 09/11/2008 | Physio Control, Inc. |
LIFEPAK 12 defibrillator/ monitors biphasic | 2 | 02/03/2005 | Medtronic Emergency Response Systems, Inc. |
LIFEPAK 12 defibrillator/monitor is a portable, battery operated, complete acute cardiac care respon... | 2 | 02/05/2003 | Medtronic Physio Control Corp |
-