Medical Device Recalls
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1 result found
510(K) Number: K200434 |
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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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AVSM3 SNF, Vital Signs Monitor The monitor is intended to be used to monitor noninvasive blood pr... | 2 | 07/19/2021 | Mediana Co., Ltd. |
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