FDA 510(k) Application Details - K160472

Device Classification Name	Lenses, Soft Contact, Daily Wear   More FDA Info for this Device
510(K) Number	K160472
Device Name	Lenses, Soft Contact, Daily Wear
Applicant	SOLOTICA R DOMINGOS FASOLARI 110 -CASA VERDE SAO PAULO 02513-010 BR Other 510(k) Applications for this Company
Contact	Gilberto Zablith Other 510(k) Applications for this Contact
Regulation Number	886.5925   More FDA Info for this Regulation Number
Classification Product Code	LPL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/19/2016
Decision Date	08/10/2016
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OP - Ophthalmic
Review Advisory Committee	OP - Ophthalmic
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review