K-number	K231202
Device name	QuickRayPRO
Applicant	Denterprise International, Inc.
Product code	MUH
Device class	Class II
Decision date	Jun 22, 2023
Decision	Substantially Equivalent
Regulation	872.1800

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Source

View the full FDA submission: accessdata.fda.gov

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QuickRayPRO

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