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.. Device class: 2.

Clearance details

Applicant: Dia Imaging Analysis, Ltd.
Product code: Code QIH
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 2022-09-27
Decision date: 2023-02-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Beer-Sheva, IL

Download summary PDF View on FDA.gov ↗

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More clearances from Dia Imaging Analysis, Ltd.

K243862 — LVivo Software Application2025-03-17
K243331 — LVivo Seamless2025-03-06
K243235 — LVivo Software Application2025-03-03
K240553 — LVivo Software Application2024-10-04
K240769 — LVivo IQS2024-05-24

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