VUNO Med-Chest X-ray Triage/VUNO Med-CXR Link Triage
K-Number: K241439 · 2024-11-15
ApplicantVuno, Inc.
Decision Date2024-11-15
Product CodeQFM
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
VUNO Med-Chest X-ray Triage/VUNO Med-CXR Link Triage is a medical device manufactured by Vuno, Inc.. It received FDA 510(k) clearance on 2024-11-15 under approval number K241439. The device is classified under product code QFM. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the VUNO Med-Chest X-ray Triage/VUNO Med-CXR Link Triage?
VUNO Med-Chest X-ray Triage/VUNO Med-CXR Link Triage is a medical device that received FDA 510(k) clearance on 2024-11-15. It is manufactured by Vuno, Inc.. The 510(k) number is K241439.
When was VUNO Med-Chest X-ray Triage/VUNO Med-CXR Link Triage approved by the FDA?
VUNO Med-Chest X-ray Triage/VUNO Med-CXR Link Triage received FDA 510(k) clearance on 2024-11-15, under approval number K241439.
What company makes VUNO Med-Chest X-ray Triage/VUNO Med-CXR Link Triage?
VUNO Med-Chest X-ray Triage/VUNO Med-CXR Link Triage is manufactured by Vuno, Inc..
What is the FDA product code for VUNO Med-Chest X-ray Triage/VUNO Med-CXR Link Triage?
The FDA product code for VUNO Med-Chest X-ray Triage/VUNO Med-CXR Link Triage is QFM.
Other Devices by Vuno, Inc.
Related Devices (Code: QFM)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.