VEA Align— 510(k) K231917

Substantially Equivalent

Eos Imaging

FDA 510(k) clearance K231917 for VEA Align, Substantially Equivalent on 2024-01-05. Applicant: Eos Imaging. Device class: 2.

Clearance details

Applicant: Eos Imaging
Product code: Code QIH
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 2023-06-29
Decision date: 2024-01-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Paris, FR

Download summary PDF View on FDA.gov ↗

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