K-number	K153027
Device name	Cryotop US
Applicant	Kitazato Biopharma Co., Ltd.
Product code	MQK
Device class	Class II
Decision date	Mar 14, 2016
Decision	Substantially Equivalent
Regulation	884.6160

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View the full FDA submission: accessdata.fda.gov

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Cryotop US

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