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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K223263
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3M Prevena Plus 125 Therapy Unit and System Kits REF: PRE3021US Prevena Plus Duo Peel and Place 20... 2 02/14/2025 FEI # 3009897021
KCI USA, INC.
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