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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K171454
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Recall
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ORISE ProKnife Procedure Kits: indicated for use in gastrointestinal endoscopic procedures for submu... 2 11/11/2022 Boston Scientific Corporation
ORISE Gel Syringe Submucosal Lifting Agent Kits: indicated for use in gastrointestinal endoscopic p... 2 11/11/2022 Boston Scientific Corporation
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