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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: K203069
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HydroMID 4Fr Single Lumen Maximal Barrier Kit-indicated for short term access (<30days) to the per... 2 02/22/2023 Access Vascular, Inc
HydroMID 4Fr Single Lumen Maximal Barrier Kit- Indicated for short term access (<30days) to the pe... 2 02/22/2023 Access Vascular, Inc
HydroMID 4Fr Single Lumen - Basic Kit, Model Number 80004002 2 02/10/2023 Access Vascular, Inc
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