K-number	K122016
Device name	REXTAR, REXTAR LCD
Applicant	Meta Biomed, Inc.
Product code	EHD
Device class	Class II
Decision date	Mar 1, 2013
Decision	Substantially Equivalent
Regulation	872.1800

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View the full FDA submission: accessdata.fda.gov

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REXTAR, REXTAR LCD

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