K241649
- 510(k) number
- K241649
- Device name
- DUO1 and DUO2
- Applicant
- Zinnovi, Inc. IL · US
- Product code
- MUH — System, X-Ray, Extraoral Source, Digital
- Decision date
- 2024-07-05
- Date received
- 2024-06-07
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Flag
- Third-party review
- Advisory committee
- Dental
510(k) Summary (official FDA PDF): K241649.pdf
Official FDA record: K241649
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.