K232255
- 510(k) number
- K232255
- Device name
- EZSensor XHD
- Applicant
- Qpix Solutions, Inc. NC · US
- Product code
- MUH — System, X-Ray, Extraoral Source, Digital
- Decision date
- 2023-09-27
- Date received
- 2023-07-28
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K232255.pdf
Official FDA record: K232255
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.