NUFACE PLUS


Device Classification Name

stimulator, transcutaneous electrical, aesthetic purposes

510(k) Number K103472
Device Name NUFACE PLUS
Applicant
Carol Cole Company
16405 summer sage rd
poway, 
CA 
92064

Applicant Contact bob duffy
Correspondent
Carol Cole Company
16405 summer sage rd
poway, 
CA 
92064

Correspodent Contact bob duffy
Regulation Number 882.5890
Classification Product Code
NFO  
Date Received 11/24/2010
Decision Date 11/07/2011
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Neurology

510k Review Panel

Neurology

summary

summary

Type Abbreviated
Reviewed by Third Party No

Combination Product

No