K-number	K202119
Device name	AcuSee AS-P1000 System
Applicant	Weipeng (Suzhou) Medical Devices Co., Ltd.
Product code	IYO
Device class	Class II
Decision date	Oct 7, 2020
Decision	Substantially Equivalent
Regulation	892.1560

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Source

View the full FDA submission: accessdata.fda.gov

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AcuSee AS-P1000 System

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