K-number	K173088
Device name	Vitrea Software Toshiba Package VSTP-001A
Applicant	Toshibamedical Systems Corporation
Product code	LLZ
Device class	Class II
Decision date	Jan 31, 2018
Decision	Substantially Equivalent
Regulation	892.2050

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View the full FDA submission: accessdata.fda.gov

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Vitrea Software Toshiba Package VSTP-001A

Everything you need for a 510(k) submission. Nothing you don't.