K-number	K132646
Device name	SUNETICS CLINICAL BIO-STIMULATION LASER
Applicant	Sunetics International Marketing Group, LLC
Product code	OAP
Device class	Class II
Decision date	Dec 20, 2013
Decision	Substantially Equivalent
Regulation	890.5500

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View the full FDA submission: accessdata.fda.gov

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SUNETICS CLINICAL BIO-STIMULATION LASER

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