K-number	K161919
Device name	UltraScan 650
Applicant	Cyberlogic, Inc.
Product code	MUA
Device class	Class II
Decision date	Apr 5, 2017
Decision	Substantially Equivalent
Regulation	892.1180

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Source

View the full FDA submission: accessdata.fda.gov

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UltraScan 650

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