Viz LVO ContaCT— 510(k) K223042

Substantially Equivalent

Viz. Ai, Inc.

FDA 510(k) clearance K223042 for Viz LVO ContaCT, Substantially Equivalent on 2022-10-21. Applicant: Viz. Ai, Inc.. Device class: 2.

Clearance details

Applicant: Viz. Ai, Inc.
Product code: Code QAS
Device class: Class 2
Regulation: 21 CFR 892.2080
Advisory panel: Radiology
Date received: 2022-09-29
Decision date: 2022-10-21
Decision: Substantially Equivalent
Clearance type: Special
Location: San Francisco, CA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Viz. Ai, Inc.

K250354 — Viz Subdural+, Viz SUBDURAL PLUS2025-06-10
K232363 — Viz HDS, Viz Volume Plus, Viz ICH+2024-02-05
DEN230003 — Viz HCM2023-08-03
K223443 — Viz AAA2023-03-17
K221100 — Viz RV/LV2022-08-29

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