K-number	K111733
Device name	CORELEADER SCAR-DIMMER
Applicant	Coreleader Biotech Co., Ltd.
Product code	MDA
Device class	Class I
Decision date	Sep 22, 2011
Decision	Substantially Equivalent
Regulation	878.4025

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View the full FDA submission: accessdata.fda.gov

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CORELEADER SCAR-DIMMER

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