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FDA 510(k), K222386, Visionbody
FDA 510(k), K222386, Visionbody
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510(K) Number: K222386
Device Name: Visionbody
Manufacturer: Jorge Millan
Device Classification Name: Stimulator, Muscle, Powered, For Muscle Conditioning
Regulation Number: NGX
Classification Product Code: 08/08/2022
Date Received: 02/24/2023
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Physical Medicine
Device Name: Visionbody
Manufacturer: Jorge Millan
Device Classification Name: Stimulator, Muscle, Powered, For Muscle Conditioning
Regulation Number: NGX
Classification Product Code: 08/08/2022
Date Received: 02/24/2023
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Physical Medicine
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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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