510(k) K231202

Device
QuickRayPRO
Applicant
Denterprise International, Inc.
510(k) number
K231202
Product code
MUH
Decision
Substantially Equivalent (SESE)
Decision date
2023-06-22
Date received
2023-04-27
Regulation
872.1800
Classification name
System, X-Ray, Extraoral Source, Digital
Medical specialty
Dental
Review panel
Dental
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No

Related Records

Applicant Contact

Contact
Claude Berthoin
Address
156 E. Granada Blvd. Ormond Beach FL US 32176 32176

FDA Registration Numbers

Source Documents

510(k) summary PDF not indicated by FDA

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