K-number	K142172
Device name	LIGHTMED TRUSCAN 577
Applicant	Lightmed Corp.
Product code	HQF
Device class	Class II
Decision date	Feb 27, 2015
Decision	Substantially Equivalent
Regulation	886.4390

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Source

View the full FDA submission: accessdata.fda.gov

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LIGHTMED TRUSCAN 577

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