Medical Device Recalls
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1 result found
510(K) Number: K060559 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ZOLL R Series Defibrillator/Pacemaker/Monitor Used by qualified medical personnel for the purpose... | 2 | 09/29/2009 | ZOLL Medical Corporation, World Wide Headquarters |
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