Ventoux VC2; Ventoux VC3
K-Number: K223120 · 2024-12-02
ApplicantFlight Medical Innovations , Ltd.
Decision Date2024-12-02
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent
Device Summary
Ventoux VC2; Ventoux VC3 is a medical device manufactured by Flight Medical Innovations , Ltd.. It received FDA 510(k) clearance on 2024-12-02 under approval number K223120. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
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. It is manufactured by Flight Medical Innovations , Ltd.. The 510(k) number is K223120.
When was Ventoux VC2; Ventoux VC3 approved by the FDA?
Ventoux VC2; Ventoux VC3 received FDA 510(k) clearance on 2024-12-02, under approval number K223120.
What company makes Ventoux VC2; Ventoux VC3?
Ventoux VC2; Ventoux VC3 is manufactured by Flight Medical Innovations , Ltd..
What is the FDA product code for Ventoux VC2; Ventoux VC3?
The FDA product code for Ventoux VC2; Ventoux VC3 is CBK.
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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.