K-number	K101838
Device name	VTS1000
Applicant	Vuetek Scientific, LLC
Product code	KZA
Device class	Class I
Decision date	Feb 18, 2011
Decision	Substantially Equivalent
Regulation	880.6970

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Source

View the full FDA submission: accessdata.fda.gov

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VTS1000

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