K-number	K142799
Device name	Model BT-220L and BT-220C
Applicant	Bistos Co., Ltd.
Product code	HGM
Device class	Class II
Decision date	Jul 9, 2015
Decision	Substantially Equivalent
Regulation	884.2740

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Source

View the full FDA submission: accessdata.fda.gov

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Model BT-220L and BT-220C

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