FDA 510(k)

LungVision

K-Number: K240943 · 2024-10-01

Decision Date2024-10-01

Product CodeQIH

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

LungVision is the device name listed in this FDA 510(k) record. The listed applicant is Bodyvision Medical , Ltd.. It received FDA 510(k) clearance on 2024-10-01 under 510(k) 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. The listed applicant is Bodyvision Medical , Ltd.. The 510(k) number is K240943.

When did LungVision receive FDA 510(k) clearance?

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

Who is the listed applicant for LungVision?

The FDA 510(k) record lists Bodyvision Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LungVision?

The FDA product code for LungVision is QIH.

Other records listing Bodyvision Medical , 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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.