FDA 510(k) Application Details - K031774

Device Classification Name	Lenses, Soft Contact, Daily Wear   More FDA Info for this Device
510(K) Number	K031774
Device Name	Lenses, Soft Contact, Daily Wear
Applicant	WESTCON CONTACT LENS CO., INC. 611 EISENHAUER ST. GRAND JUNCTION, CO 81505 US Other 510(k) Applications for this Company
Contact	CAROL NOBEL 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	06/09/2003
Decision Date	02/20/2004
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