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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K172040
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Aquilex Fluid Control System-Intended to provide fluid distension of the uterus during diagnostic an... 2 01/05/2024 FEI # 3002914049
WOM World Of Medicine AG
Aquilex Fluid Control System component: Bag deflector, REF AQL-100CBS Product Usage: Distends ... 2 09/30/2019 FEI # 3001556604
WOM World of Medicine AG
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