FDA 510(k) Application Details - K162223

Device Classification Name	Lenses, Soft Contact, Daily Wear   More FDA Info for this Device
510(K) Number	K162223
Device Name	Lenses, Soft Contact, Daily Wear
Applicant	SUPERVISION OPTIMAX SDN BHD LOT 38, PUTRA INDUSTRIAL PARK, BUKIT RAHMAN PUTRA SUNGAI BULOH 40160 MY Other 510(k) Applications for this Company
Contact	YAP PEAK GEEH 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	08/08/2016
Decision Date	01/04/2017
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OP - Ophthalmic
Review Advisory Committee	OP - Ophthalmic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review