K-number	K130581
Device name	KONIX STERILE GEL
Applicant	Turkuaz Saglik Hizmetleri Medikal Temizlik Kimyasa
Product code	MUI
Device class	Class II
Decision date	Jun 18, 2014
Decision	Substantially Equivalent
Regulation	892.1570

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View the full FDA submission: accessdata.fda.gov

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KONIX STERILE GEL

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