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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name Epilator, High Frequency, Tweezer-Type
510(k) Number K761049
Device Name KENATRON EPILATOR
Applicant
EPILATOR CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
EPILATOR CORP.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number878.5360
Classification Product Code
KCX  
Date Received11/15/1976
Decision Date 01/05/1977
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
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