FDA 510(k) Application Details - K052703

Device Classification Name	Lenses, Soft Contact, Daily Wear   More FDA Info for this Device
510(K) Number	K052703
Device Name	Lenses, Soft Contact, Daily Wear
Applicant	ALDEN OPTICAL LABS., INC. 13295 BROADWAY ALDEN, NY 14004 US Other 510(k) Applications for this Company
Contact	CHARLES H CREIGHTON 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	09/28/2005
Decision Date	11/10/2005
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OP - Ophthalmic
Review Advisory Committee	OP - Ophthalmic
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review