Medical Device Recalls
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1 result found
510(K) Number: K170497 |
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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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| DIRECT SUPPLY Attendant VITAL SIGNS MONITOR, REF AVSM2 - Product Usage: It is vital sign monitor to ... | 2 | 06/26/2020 |
FEI # 3003591740 Mediana Co., Ltd. |
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