K-number	K151309
Device name	Wartie Advanced Wart Remover or other proprietary name
Applicant	Youmedical Corp BV
Product code	GEH
Device class	Class II
Decision date	Aug 14, 2015
Decision	Substantially Equivalent
Regulation	878.4350

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Source

View the full FDA submission: accessdata.fda.gov

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Wartie Advanced Wart Remover or other proprietary name

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