K233053
- 510(k) number
- K233053
- Device name
- DEXIS Ti2 Intraoral Sensor, DEXIS IXS Size 1 Intraoral Sensor, DEXIS IXS Size 2 Intraoral Sensor
- Applicant
- Dental Imaging Technologies Corporation PA · US
- Product code
- MUH — System, X-Ray, Extraoral Source, Digital
- Decision date
- 2023-11-21
- Date received
- 2023-09-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K233053.pdf
Official FDA record: K233053
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.