K-number	K131007
Device name	AIGIS RX N MEDIUM; AIGIS RX N LARGE
Applicant	Tyrx, Inc.
Product code	FTL
Device class	Class II
Decision date	Jul 10, 2013
Decision	Substantially Equivalent
Regulation	878.3300

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View the full FDA submission: accessdata.fda.gov

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AIGIS RX N MEDIUM; AIGIS RX N LARGE

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