K-number	K001223
Device name	ACULUX, MODEL AX3001, AX3002
Applicant	Aculux
Product code	FQP
Device class	Class II
Decision date	Jun 23, 2000
Decision	Substantially Equivalent
Regulation	878.4580

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View the full FDA submission: accessdata.fda.gov

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ACULUX, MODEL AX3001, AX3002

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