Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Vuno, Inc.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories2
Latest FDA decision2024-11-15
TypeNumberDevice NameCodeDateActions
510(k) K241439 VUNO Med-Chest X-ray Triage/VUNO Med-CXR Link TriageQFM2024-11-15 View
510(k) K231398 VUNO Med-DeepBrainQIH2023-10-04 View