HEMASHIELD WOVEN DOUBLE VELOUR VASCULAR GRAFT MODEL M00202175XXXXX; M00202166XXXXX (K122612) — FDA 510(k) Clearance | Predicase

K-number	K122612
Device name	HEMASHIELD WOVEN DOUBLE VELOUR VASCULAR GRAFT MODEL M00202175XXXXX; M00202166XXXXX
Applicant	Maquet Cardiovascular, LLC
Product code	MAL
Device class	Class II
Decision date	Sep 10, 2012
Decision	Substantially Equivalent
Regulation	870.3450

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Source

View the full FDA submission: accessdata.fda.gov

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