Clearance Summary
InVision 3T Recharge Operating Suite received FDA 510(k) clearance under submission number K252239, sponsored by Imris Imaging, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2025-08-06.
- Submission: K252239
- Applicant / Sponsor: Imris Imaging, Inc.
- Clearance pathway: Traditional
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1000
- Decision date: 2025-08-06
Classification & Regulation
This clearance is catalogued under FDA product code LNH and 21 CFR 892.1000, within the Radiology review panel as a Class II device.