Medical Device Recalls
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1 result found
510(K) Number: K091238 |
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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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731 Series Ventilators running software version 05.20.00 The devices in the ZOLL ventilator are ... | 2 | 03/01/2018 | ZOLL Medical Corporation |
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