K-number	K172602
Device name	Miracu
Applicant	Feeltech Co., Ltd.
Product code	NEW
Device class	Class II
Decision date	Nov 14, 2018
Decision	Substantially Equivalent
Regulation	878.4840

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Source

View the full FDA submission: accessdata.fda.gov

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Miracu

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