FDA 510(k), K161654, NuFACE Gel Primer

FDA 510(k), K161654, NuFACE Gel Primer

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510(K) Number: K161654
Device Name: NuFACE Gel Primer
Manufacturer: Carol Cole Company
Device Classification Name: media, electroconductive
Regulation Number: 882.1275
Classification Product Code: GYB
Date Received: 06/15/2016
Decision Date: 12/30/2016
Regulation Medical Specialty: Neurology

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