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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: K172319
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AMSCO V-PRO 1, V-PRO 1 Plus, and V-PRO maX Low Temperature Sterilization Systems The V-PRO 1, V-... 2 08/31/2018 FEI # 1527821
Steris Corporation
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