K-number	K092446
Device name	INTRA LUX HEAD 3 LDSY
Applicant	Kaltenbach & Voigt GmbH & Co.
Product code	EFA
Device class	Class I
Decision date	Nov 3, 2009
Decision	Substantially Equivalent
Regulation	872.4200

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View the full FDA submission: accessdata.fda.gov

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INTRA LUX HEAD 3 LDSY

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