FDA 510(k) Application Details - K110301

Device Classification Name	Light Based Over The Counter Wrinkle Reduction   More FDA Info for this Device
510(K) Number	K110301
Device Name	Light Based Over The Counter Wrinkle Reduction
Applicant	HOME SKINOVATIONS LTD. TAVOR BULD. POB 533 YOKNEAM ILLIT 20692 IL Other 510(k) Applications for this Company
Contact	AMIR WALDMAN PH. D. Other 510(k) Applications for this Contact
Regulation Number	878.4810   More FDA Info for this Regulation Number
Classification Product Code	OHS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/02/2011
Decision Date	08/19/2011
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