K221275
- 510(k) number
- K221275
- Device name
- Qraycam PRO
- Applicant
- AIOBIO Co., Ltd. KR
- Product code
- NBL — Light-Induced Fluorescence Caries Detector
- Decision date
- 2024-09-04
- Date received
- 2022-05-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K221275.pdf
Official FDA record: K221275
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.