K-number	K092291
Device name	SKINTACT AND VARIOUS OTHER TRADENAMES
Applicant	Leonhard Lang GmbH
Product code	DRX
Device class	Class II
Decision date	Aug 21, 2009
Decision	Substantially Equivalent
Regulation	870.2360

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Source

View the full FDA submission: accessdata.fda.gov

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SKINTACT AND VARIOUS OTHER TRADENAMES

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