K-number	K112989
Device name	AQUILION CXL
Applicant	Toshiba America Medical Systems, In.C
Product code	JAK
Device class	Class II
Decision date	Apr 10, 2012
Decision	Substantially Equivalent
Regulation	892.1750

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Source

View the full FDA submission: accessdata.fda.gov

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AQUILION CXL

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