Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K010918 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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The LIFEPAK12 Defibrillator/Monitor. The LIFEPAK12 Defibrillator/Monitor can be used in AED mode, m... | 2 | 03/04/2011 | Physio Control, Inc. |
LIFEPAK 12 defibrillator/monitor | 2 | 04/04/2006 | Medtronic Emergency Response Systems, Inc. |
Hard shell carry case for the LIFEPAK 500 AED. | 2 | 10/04/2005 | 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 |
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