K-number	K192192
Device name	VSP System
Applicant	3D Systems
Product code	DZJ
Device class	Class II
Decision date	Feb 26, 2020
Decision	Substantially Equivalent
Regulation	872.4120

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Source

View the full FDA submission: accessdata.fda.gov

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VSP System

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