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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: K052302
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HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-Thoracoabdominal, Product Code: M00202175426T... 2 05/04/2020 FEI # 2242352
Maquet Cardiovascular, LLC
HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-Thoracoabdominal, Product Code: M00202175428T... 2 05/04/2020 FEI # 2242352
Maquet Cardiovascular, LLC
Hemashield Platinum Woven Double Velour TAAA Vascular Grafts. 2 07/22/2010 FEI # 2242352
Maquet Cardiovascular, LLC
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