Devices · QT Imaging Holdings, Inc.
QT Scanner 2000 Model A
510(k)K253898RadiologyIYO
QT Imaging Holdings, Inc. is listed for QT Scanner 2000 Model A (K253898). The FDA list gives March 4, 2026 as the date of the final decision. The lead panel is Radiology, and the database link on the FDA list is the 510(k) pathway. The primary product code on the FDA list is IYO. openFDA did not return a classification record for that code in this copy of the data. openFDA records this submission’s decision description as “Substantially Equivalent.” This paragraph is assembled only from those public fields. It is not an FDA review, not a determination of safety or effectiveness, and not medical advice. Official record: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMN/pmn.cfm?ID=K253898
- Date of final decision
- March 4, 2026
- Company on the FDA list
- QT Imaging Holdings, Inc.
- Lead panel
- Radiology
- Primary product code
- IYO
- openFDA device name for the code
- System, Imaging, Pulsed Echo, Ultrasonic
- Device class
- 2
- Regulation number
- 892.1560
- openFDA decision description
- Substantially Equivalent
- openFDA decision code
- SESE
- Statement or summary label
- Summary