510(k) K241649

Device
DUO1 and DUO2
Applicant
Zinnovi, Inc.
510(k) number
K241649
Product code
MUH
Decision
Substantially Equivalent (SESE)
Decision date
2024-07-05
Date received
2024-06-07
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
Summary
Third party reviewed
Yes

Related Records

Applicant Contact

Contact
Swaroop Patel
Address
135 W. Central Rd. Suite 204 Schaumburg IL US 60195 60195

FDA Registration Numbers

Source Documents

510(k) summary PDF

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