K-number	K113311
Device name	TIO2MESH TM
Applicant	Biocer Entwicklungs GmbH
Product code	FTL
Device class	Class II
Decision date	Jul 17, 2012
Decision	Substantially Equivalent
Regulation	878.3300

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View the full FDA submission: accessdata.fda.gov

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TIO2MESH TM

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