K-number	K081116
Device name	G-IVF G5 SERIES
Applicant	Vitrolife Sweden AB
Product code	MQL
Device class	Class II
Decision date	Sep 2, 2008
Decision	Substantially Equivalent
Regulation	884.6180

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View the full FDA submission: accessdata.fda.gov

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G-IVF G5 SERIES

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