K-number	K132699
Device name	AIGIS RX N (MEDIUM), AIGIS RX N (LARGE)
Applicant	Tyrx, Inc.
Product code	FTL
Device class	Class II
Decision date	Nov 26, 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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