Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K082937 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| The LIFEPAK 15 monitor/defibrillator is intended for use by trained medical personnel in outdoor an... | 2 | 12/14/2016 | Physio-Control, Inc. |
| Biphasic LIFEPAK 15 Monitor/Defibrillator. The LIFEPAK 15 is a battery operated monitor with an e... | 2 | 09/18/2009 | Physio Control, Inc. |
| Biphasic LIFEPAK 15 Monitor/Defibrillator. Manufactured by Physio-Control Inc., a division of Medtr... | 1 | 04/21/2010 | Physio Control, Inc. |
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