K-number	K001179
Device name	SUPER NOVA, ACUBEAM
Applicant	Light Force Therapy, Inc.
Product code	ILY
Device class	Class II
Decision date	Oct 27, 2000
Decision	Substantially Equivalent
Regulation	890.5500

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View the full FDA submission: accessdata.fda.gov

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SUPER NOVA, ACUBEAM

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