FDA 510(k) Application Details - K090221

Device Classification Name	Massager, Vacuum, Light Induced Heating   More FDA Info for this Device
510(K) Number	K090221
Device Name	Massager, Vacuum, Light Induced Heating
Applicant	VIORA LTD. 30 MONTGOMERY STREET SUITE 660 JERSEY CITY, NJ 07302 US Other 510(k) Applications for this Company
Contact	JOSEF LUZON Other 510(k) Applications for this Contact
Regulation Number	878.4810   More FDA Info for this Regulation Number
Classification Product Code	NUV Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/30/2009
Decision Date	07/01/2009
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