Medical Device Recalls
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1 result found
510(K) Number: K183543 |
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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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ACTIV.A.C Therapy System; Model Numbers; US: 340000 ACTIV.A.C., NORTH AMERICAN UDI (01)00878237008... | 2 | 07/10/2020 | KCI USA, INC. |
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