K-number	K073352
Device name	WEBERNEEDLE BASIC LASER
Applicant	Weber Medical GmbH
Product code	ILY
Device class	Class II
Decision date	Aug 11, 2008
Decision	Substantially Equivalent
Regulation	890.5500

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Source

View the full FDA submission: accessdata.fda.gov

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WEBERNEEDLE BASIC LASER

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