K-number	K161670
Device name	Lucid Q-PTP / HWA 55
Applicant	Bison Medical Co, Ltd.
Product code	GEX
Device class	Class II
Decision date	Nov 2, 2016
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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Lucid Q-PTP / HWA 55

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