K-number	K131822
Device name	ULTRAEXTEND USWS-900A V2.1 AND V3.1
Applicant	Toshiba America Medical Systems, In.C
Product code	LLZ
Device class	Class II
Decision date	Jul 23, 2013
Decision	Substantially Equivalent
Regulation	892.2050

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View the full FDA submission: accessdata.fda.gov

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ULTRAEXTEND USWS-900A V2.1 AND V3.1

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