Medical Device Recalls
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1 result found
510(K) Number: K112761 |
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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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Zoll Medical X Series, PropaqMD, PropaqM Defibrillator/Pacemaker/Monitor With System Software Ver... | 2 | 03/31/2014 | ZOLL Medical Corporation |
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