Lung Vision System
K-Number: K183593 · 2019-04-18
ApplicantBodyvision Medical , Ltd.
Decision Date2019-04-18
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Lung Vision System is a medical device manufactured by Bodyvision Medical , Ltd.. It received FDA 510(k) clearance on 2019-04-18 under approval number K183593. 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 System?
Lung Vision System is a medical device that received FDA 510(k) clearance on 2019-04-18. It is manufactured by Bodyvision Medical , Ltd.. The 510(k) number is K183593.
When was Lung Vision System approved by the FDA?
Lung Vision System received FDA 510(k) clearance on 2019-04-18, under approval number K183593.
What company makes Lung Vision System?
Lung Vision System is manufactured by Bodyvision Medical , Ltd..
What is the FDA product code for Lung Vision System?
The FDA product code for Lung Vision System is LLZ.
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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.