FDA 510(k) Application Details - K952260

Device Classification Name	Lens, Contact (Other Material) - Daily   More FDA Info for this Device
510(K) Number	K952260
Device Name	Lens, Contact (Other Material) - Daily
Applicant	STELLAR CONTACT LENS, INC. 203 N. WABASH AVE, STE 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	886.5916   More FDA Info for this Regulation Number
Classification Product Code	HQD Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/15/1995
Decision Date	01/03/1996
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