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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: K241550
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Gelsoft Plus, REF: 635024PE, 631514PE, 631222PE, 633008PE, 633010PE, 633007PE, 636010PE, 632522PE, 6... 2 03/04/2026 FEI # 3002808437
Vascutek, Ltd.
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