FDA 510(k)

Lung Vision

K-Number: K163622 · 2017-05-11

Decision Date2017-05-11

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

Lung Vision 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 2017-05-11 under 510(k) number K163622. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Lung Vision?

Lung Vision is a medical device that received FDA 510(k) clearance on 2017-05-11. The listed applicant is Bodyvision Medical , Ltd.. The 510(k) number is K163622.

When did Lung Vision receive FDA 510(k) clearance?

Lung Vision received FDA 510(k) clearance on 2017-05-11, under 510(k) number K163622.

Who is the listed applicant for Lung Vision?

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 Lung Vision?

The FDA product code for Lung Vision is LLZ.

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.

K240943LungVision K183593Lung Vision System K172955LungVision Tool

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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.