K-number	K101003
Device name	RAPIDVIT BLAST, RAPIDWARM BLAST
Applicant	Vitrolife Sweden AB
Product code	MQL
Device class	Class II
Decision date	Dec 10, 2010
Decision	Substantially Equivalent
Regulation	884.6180

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Source

View the full FDA submission: accessdata.fda.gov

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RAPIDVIT BLAST, RAPIDWARM BLAST

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