510(k) K252091

Surgical Reality Viewer by Medicalvr B.V. — Product Code QIH

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 29, 2026
Date Received
July 3, 2025
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Automated Radiological Image Processing Software
Device Class
Class II
Regulation Number
892.2050
Review Panel
RA
Submission Type

To provide automated radiological image processing and analysis tools. Software implementing artificial intelligence including nonadaptive machine learning algorithms trained with clinical and/or artificial data. In these devices, the algorithm training data typically impacts device performance. Adaptive AI algorithms are not within scope of this product code.