FDA 510(k) Application Details - K963488

Device Classification Name	Lenses, Soft Contact, Daily Wear   More FDA Info for this Device
510(K) Number	K963488
Device Name	Lenses, Soft Contact, Daily Wear
Applicant	SPECIALTY ULTRAVISION, INC. 307 ORCHARD CITY DR. SUITE 100 CAMPBELL, CA 95008 US Other 510(k) Applications for this Company
Contact	GARY EDWARDS 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	09/03/1996
Decision Date	11/20/1996
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