Lung Vision
K-Number: K163622 · 2017-05-11
ApplicantBodyvision Medical , Ltd.
Decision Date2017-05-11
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Lung Vision is a medical device manufactured by Bodyvision Medical , Ltd.. It received FDA 510(k) clearance on 2017-05-11 under approval 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. It is manufactured by Bodyvision Medical , Ltd.. The 510(k) number is K163622.
When was Lung Vision approved by the FDA?
Lung Vision received FDA 510(k) clearance on 2017-05-11, under approval number K163622.
What company makes Lung Vision?
Lung Vision is manufactured by Bodyvision Medical , Ltd..
What is the FDA product code for Lung Vision?
The FDA product code for Lung Vision is LLZ.
Other Devices by Bodyvision Medical , Ltd.
Related Devices (Code: LLZ)
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.