FDA 510(k) Application Details - K973773

Device Classification Name	Epilator, High Frequency, Tweezer-Type   More FDA Info for this Device
510(K) Number	K973773
Device Name	Epilator, High Frequency, Tweezer-Type
Applicant	WELLQUEST INTL., INC. 230 FIFTH AVE, NEW YORK, NY 10001 US Other 510(k) Applications for this Company
Contact	STEVEN MISHAN 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	10/02/1997
Decision Date	12/17/1997
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review