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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: K013172
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X-Flow prostatectomy catheter, Device Reference Numbers AB6022, AB6024, AB6118, AB6120, AB6122, AB61... 2 01/10/2025 FEI # 2125050
Coloplast Manufacturing US, LLC
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