K-number	K141869
Device name	QFLOW 500 TITANIUM BOLT, QUAD LUMEN BOLT KIT
Applicant	Hemedex Incorporated
Product code	GWM
Device class	Class II
Decision date	Oct 10, 2014
Decision	Substantially Equivalent
Regulation	882.1620

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View the full FDA submission: accessdata.fda.gov

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QFLOW 500 TITANIUM BOLT, QUAD LUMEN BOLT KIT

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