Ventoux VC2; Ventoux VC3— 510(k) K223120

Substantially Equivalent

Flight Medical Innovations , Ltd.

FDA 510(k) clearance K223120 for Ventoux VC2; Ventoux VC3, Substantially Equivalent on 2024-12-02. Applicant: Flight Medical Innovations , Ltd..

Clearance details

Applicant: Flight Medical Innovations , Ltd.
Product code: Code CBK
Advisory panel: Anesthesiology
Date received: 2022-10-03
Decision date: 2024-12-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Petach Tikva, IL

Download summary PDF View on FDA.gov ↗

Adverse events under product code CBK

product code CBK

Death: 736
Injury: 3,628
Malfunction: 98,786
Other: 4
Total: 103,154

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.