K-number	K082727
Device name	FOLLICLE ASPIRATION SET, REDUCED SINGLE LUMEN
Applicant	Vitrolife Sweden AB
Product code	MQE
Device class	Class II
Decision date	Feb 6, 2009
Decision	Substantially Equivalent
Regulation	884.6100

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View the full FDA submission: accessdata.fda.gov

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FOLLICLE ASPIRATION SET, REDUCED SINGLE LUMEN

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