Epilator Corporation


Epilator Corporation

Almost nothing is known about the manufacturer of this electric tweezer scam at the time of this writing.

Contact information

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Available devices

Epilator name FDA 510(k) Cleared
     

Notes

 

Device Classification Name
EPILATOR, HIGH FREQUENCY, TWEEZER-TYPE
Regulation Number
878.5360
510(k) Number
K761049
Device Name
KENATRON EPILATOR
Applicant
EPILATOR CORP.
Product Code
KCX
Date Received
11/15/76
Decision Date
01/05/77
Decision
Substantially Equivalent
Classification Advisory Committee
General & Plastic Surgery
Review Advisory Committee
General & Plastic Surgery
Statement/Summary/Purged Indicator
Purged, no summary or statement
Type
Traditional