K-number	K172331
Device name	Type I, Type II, Type III, Type IV
Applicant	Lepu Medical Technology (Beijing) Co., Ltd.
Product code	DYB
Device class	Class II
Decision date	Mar 2, 2018
Decision	Unknown
Regulation	870.1340

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Source

View the full FDA submission: accessdata.fda.gov

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Type I, Type II, Type III, Type IV

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