Cleared Traditional

VUNO Med-Chest X-ray Triage/VUNO Med-CXR Link Triage

K241439 · Vuno, Inc. · Radiology
Nov 2024
Decision
178d
Days
Class 2
Risk

About This 510(k) Submission

K241439 is an FDA 510(k) clearance for the VUNO Med-Chest X-ray Triage/VUNO Med-CXR Link Triage, a Radiological Computer-assisted Prioritization Software For Lesions (Class II — Special Controls, product code QFM), submitted by Vuno, Inc. (Seoul, KR). The FDA issued a Cleared decision on November 15, 2024, 178 days after receiving the submission on May 21, 2024. This device falls under the Radiology review panel. Regulated under 21 CFR 892.2080.

Submission Details

510(k) Number K241439 FDA.gov
FDA Decision Cleared SESE
Date Received May 21, 2024
Decision Date November 15, 2024
Days to Decision 178 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF

Device Classification

Product Code QFM — Radiological Computer-assisted Prioritization Software For Lesions
Device Class Class II — Special Controls
CFR Regulation 21 CFR 892.2080
Definition Radiological Computer-assisted Prioritization Software For Lesions Is An Image Processing Device Intended To Aid In Prioritization And Triage Of Time Sensitive Patient Detection And Diagnosis Based On The Analysis Of Medical Images Acquired From Radiological Signal Acquisition Systems. The Device Identifies Or Prioritizes Time Sensitive Imaging For Review By Prespecified Clinical Users Based On Software-based Image Analysis But Does Not Provide Information From The Image Analysis Other Than Triage And Notification.