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FDA 510(k), K142794, Everyway Facial MENS
FDA 510(k), K142794, Everyway Facial MENS
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510(K) Number: K142794
Device Name: Everyway Facial MENS
Manufacturer: ROBERT TU
Device Classification Name: Stimulator, Transcutaneous Electrical, Aesthetic Purposes
Regulation Number: NFO
Classification Product Code: 09/29/2014
Date Received: 06/02/2015
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Neurology
Device Name: Everyway Facial MENS
Manufacturer: ROBERT TU
Device Classification Name: Stimulator, Transcutaneous Electrical, Aesthetic Purposes
Regulation Number: NFO
Classification Product Code: 09/29/2014
Date Received: 06/02/2015
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Neurology
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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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