K-number	K202713
Device name	TrueView 100 Pro
Applicant	Compai Healthcare (Shenzhen) Co.,Ltd
Product code	MWP
Device class	Class II
Decision date	Nov 18, 2020
Decision	Substantially Equivalent
Regulation	892.1680

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Source

View the full FDA submission: accessdata.fda.gov

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TrueView 100 Pro

Everything you need for a 510(k) submission. Nothing you don't.