K-number	K161198
Device name	Lumix Ultra 1, Lumix Ultra 2, Lumix Ultra 3
Applicant	Usa Laser Biotech, Inc.
Product code	ILY
Device class	Class II
Decision date	Jul 26, 2016
Decision	Substantially Equivalent
Regulation	890.5500

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Source

View the full FDA submission: accessdata.fda.gov

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Lumix Ultra 1, Lumix Ultra 2, Lumix Ultra 3

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