Surgical Reality Viewer— 510(k) K252091

Substantially Equivalent

Medicalvr B.V.

FDA 510(k) clearance K252091 for Surgical Reality Viewer, Substantially Equivalent on 2026-01-29. Applicant: Medicalvr B.V.. Device class: 2.

Clearance details

Applicant: Medicalvr B.V.
Product code: Code QIH
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 2025-07-03
Decision date: 2026-01-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Nieuw-Vennep, NL

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.