K-number	K121267
Device name	BT-200V VASCULAR DOPPLER
Applicant	Bistos Co., Ltd.
Product code	HGM
Device class	Class II
Decision date	Aug 2, 2012
Decision	Substantially Equivalent
Regulation	884.2740

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Source

View the full FDA submission: accessdata.fda.gov

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BT-200V VASCULAR DOPPLER

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