FDA 510(k) Application Details - K990281

Device Classification Name	Lenses, Soft Contact, Daily Wear   More FDA Info for this Device
510(K) Number	K990281
Device Name	Lenses, Soft Contact, Daily Wear
Applicant	NISSEL LTD. 203 NORTH WABASH AVE. SUITE 1200 CHICAGO, IL 60601 US Other 510(k) Applications for this Company
Contact	JOHN M SZABOCSIK 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	01/28/1999
Decision Date	04/16/1999
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