K-number	K213908
Device name	SKR 3000
Applicant	Konica Minolta, Inc.
Product code	MQB
Device class	Class II
Decision date	Jan 31, 2022
Decision	Substantially Equivalent
Regulation	892.1680

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Source

View the full FDA submission: accessdata.fda.gov

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SKR 3000

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