FDA 510(k) Application Details - K972695

Device Classification Name	Epilator, High Frequency, Tweezer-Type   More FDA Info for this Device
510(K) Number	K972695
Device Name	Epilator, High Frequency, Tweezer-Type
Applicant	MEHL/GROUP MARKETING 48 MT. OLIVE RD. BUDD LAKE, NJ 07828 US Other 510(k) Applications for this Company
Contact	THOMAS BLAKE Other 510(k) Applications for this Contact
Regulation Number	878.5360   More FDA Info for this Regulation Number
Classification Product Code	KCX Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/18/1997
Decision Date	10/22/1997
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review