Medical Device Recalls
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1 result found
510(K) Number: K033275 |
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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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LIFEPAK CR Plus and/or LIFEPAK EXPRESS are Automatic External Defibrillator(s) and are non-wearable.... | 2 | 06/29/2016 | Physio-Control, Inc. |
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