FDA 510(k) Application Details - K954031

Device Classification Name	Epilator, High Frequency, Needle-Type   More FDA Info for this Device
510(K) Number	K954031
Device Name	Epilator, High Frequency, Needle-Type
Applicant	R. A. FISCHER CO. CORP. 517 COMMERCIAL ST. GLENDALE, CA 91203 US Other 510(k) Applications for this Company
Contact	MARK VAN ORDEN Other 510(k) Applications for this Contact
Regulation Number	878.5350   More FDA Info for this Regulation Number
Classification Product Code	KCW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/28/1995
Decision Date	01/05/1996
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