K-number	K102327
Device name	CLEARVISION DR 7000F
Applicant	Jpi Healthcare Co, Ltd.
Product code	MQB
Device class	Class II
Decision date	Apr 13, 2012
Decision	Substantially Equivalent
Regulation	892.1680

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View the full FDA submission: accessdata.fda.gov

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CLEARVISION DR 7000F

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