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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K162900
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Bard 3F SL PowerMidline Full Kit CE-indicated for short term access to the peripheral venous system ... 2 10/23/2020 FEI # 2243072
Becton Dickinson & Company
Bard 3F SL PowerMidline Basic Kit CE-indicated for short term access to the peripheral venous system... 2 10/23/2020 FEI # 2243072
Becton Dickinson & Company
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