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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: K990503
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Vascutek Gelsoft Vascular Graft (peripheral) Labeling reads in part, "***Gelsoft Gelatin Impregnate... 2 11/18/2013 FEI # 1828100
Terumo Cardiovascular Systems Corporation
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