Medical Device Recalls
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1 result found
510(K) Number: K110742 |
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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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OneStep CPR Complete, Adult Multi Function Electrodes, Part Numbers: 8900 0214 01 (case of 8 single ... | 2 | 03/13/2018 | ZOLL Medical Corporation |
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