Clearance Summary
IASIS i2 Relaxation Neurofeedback System received FDA 510(k) clearance under submission number K252923, sponsored by Iasis Technologies. The device was reviewed via the Traditional premarket notification pathway and assigned to the Unknown review panel. The statutory decision date of record is 2026-03-13.
- Submission: K252923
- Applicant / Sponsor: Iasis Technologies
- Clearance pathway: Traditional
- Review panel: Unknown
- Device class:
- Decision date: 2026-03-13
Classification & Regulation
This clearance is catalogued under FDA product code , within the Unknown review panel as a device.