K-number	K180663
Device name	LaVid FMTS DIAGNOSTIC X-RAY SYSTEM
Applicant	Livermoretech, Inc.
Product code	KPR
Device class	Class II
Decision date	May 18, 2018
Decision	Substantially Equivalent
Regulation	892.1680

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View the full FDA submission: accessdata.fda.gov

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LaVid FMTS DIAGNOSTIC X-RAY SYSTEM

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