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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K993933
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ARROWg+ard Blue® Two-Lumen Hemodialysis Catheterization Kit for High Volume Infusions (1) Part Numbe... 2 04/10/2018 FEI # 3015859709
Arrow International Inc
ARROWg+ard Blue Two Lumen Hemodialysis Catheterization Kit for High Volume Infusions; Product Codes:... 2 02/20/2018 FEI # 3015859709
Arrow International Inc
1) ARROWg+ard Blue You-Blend Two-Lumen Hemodialysis Catheterization Kit for High Volume Infusions T... 2 06/12/2017 FEI # 3015859709
Arrow International Inc
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