K242778
- 510(k) number
- K242778
- Device name
- X Sensor (Model: IOS-A15IF, HDI-15DGF)
- Applicant
- Qpix Solutions, Inc. NC · US
- Product code
- MUH — System, X-Ray, Extraoral Source, Digital
- Decision date
- 2024-10-11
- Date received
- 2024-09-13
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K242778.pdf
Official FDA record: K242778
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.