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FDA 510(k), K183593, Lung Vision System
FDA 510(k), K183593, Lung Vision System
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510(K) Number: K183593
Device Name: Lung Vision System
Manufacturer: Body Vision Medical Ltd.
Device Classification Name: System, Image Processing, Radiological
Regulation Number: 892.2050
Classification Product Code: LLZ
Date Received: 12/21/2018
Decision Date: 04/18/2019
Regulation Medical Specialty: Radiology
Device Name: Lung Vision System
Manufacturer: Body Vision Medical Ltd.
Device Classification Name: System, Image Processing, Radiological
Regulation Number: 892.2050
Classification Product Code: LLZ
Date Received: 12/21/2018
Decision Date: 04/18/2019
Regulation Medical Specialty: Radiology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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