Ventoux VC2; Ventoux VC3
K-Number: K223120 · 2024-12-02
Device Summary
Frequently Asked Questions
What is the Ventoux VC2; Ventoux VC3?
Ventoux VC2; Ventoux VC3 is a medical device that received FDA 510(k) clearance on 2024-12-02. The listed applicant is Flight Medical Innovations , Ltd.. The 510(k) number is K223120.
When did Ventoux VC2; Ventoux VC3 receive FDA 510(k) clearance?
Ventoux VC2; Ventoux VC3 received FDA 510(k) clearance on 2024-12-02, under 510(k) number K223120.
Who is the listed applicant for Ventoux VC2; Ventoux VC3?
The FDA 510(k) record lists Flight Medical Innovations , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Ventoux VC2; Ventoux VC3?
The FDA product code for Ventoux VC2; Ventoux VC3 is CBK.
Other records listing Flight Medical Innovations , Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: CBK)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.