K-number	K150950
Device name	FreezeKit Cleave , ThawKit Cleave
Applicant	Vitrolife Sweden AB
Product code	MQL
Device class	Class II
Decision date	Dec 21, 2015
Decision	Substantially Equivalent
Regulation	884.6180

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Source

View the full FDA submission: accessdata.fda.gov

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FreezeKit Cleave , ThawKit Cleave

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