LVivo IQS— 510(k) K222970

Substantially Equivalent

Dia Imaging Analysis, Ltd.

FDA 510(k) clearance K222970 for LVivo IQS, Substantially Equivalent on 2023-02-01. Applicant: Dia Imaging Analysis, Ltd..

Clearance details

Applicant: Dia Imaging Analysis, Ltd.
Product code: Code QIH
Advisory panel: Radiology
Date received: 2022-09-27
Decision date: 2023-02-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Beer-Sheva, IL

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