LungVision— 510(k) K240943

Substantially Equivalent

Bodyvision Medical , Ltd.

FDA 510(k) clearance K240943 for LungVision, Substantially Equivalent on 2024-10-01. Applicant: Bodyvision Medical , Ltd.. Device class: 2.

Clearance details

Applicant: Bodyvision Medical , Ltd.
Product code: Code QIH
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 2024-04-05
Decision date: 2024-10-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Herzliya, IL

Download summary PDF View on FDA.gov ↗

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