K-number	K013376
Device name	QFLOW 500 PERFUSION MONITORING SYSTEM
Applicant	Hemedex Incorporated
Product code	DPW
Device class	Class II
Decision date	May 8, 2002
Decision	Substantially Equivalent
Regulation	870.2100

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View the full FDA submission: accessdata.fda.gov

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QFLOW 500 PERFUSION MONITORING SYSTEM

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