K-number	K001477
Device name	AURELUX Y 84 PREMIUM
Applicant	Aurex SA (Pty) , Ltd.
Product code	EJT
Device class	Class II
Decision date	Jun 20, 2000
Decision	Substantially Equivalent
Regulation	872.3060

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View the full FDA submission: accessdata.fda.gov

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AURELUX Y 84 PREMIUM

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