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FDA 510(k)

LungVision

K-Number: K240943 · 2024-10-01

ApplicantBodyvision Medical , Ltd.
Decision Date2024-10-01
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LungVision is a medical device manufactured by Bodyvision Medical , Ltd.. It received FDA 510(k) clearance on 2024-10-01 under approval number K240943. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LungVision?

LungVision is a medical device that received FDA 510(k) clearance on 2024-10-01. It is manufactured by Bodyvision Medical , Ltd.. The 510(k) number is K240943.

When was LungVision approved by the FDA?

LungVision received FDA 510(k) clearance on 2024-10-01, under approval number K240943.

What company makes LungVision?

LungVision is manufactured by Bodyvision Medical , Ltd..

What is the FDA product code for LungVision?

The FDA product code for LungVision is QIH.

Other Devices by Bodyvision Medical , Ltd.

K163622Lung Vision K172955LungVision Tool K183593Lung Vision System

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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.

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