K-number	K121363
Device name	DIOWAVE LOW LEVEL COLD LASER SYSTEM
Applicant	Technological Medical Advancments, Inc. (Tma)
Product code	ILY
Device class	Class II
Decision date	Nov 23, 2012
Decision	Substantially Equivalent
Regulation	890.5500

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View the full FDA submission: accessdata.fda.gov

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DIOWAVE LOW LEVEL COLD LASER SYSTEM

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