FDA 510(k) Application Details - K061120

Device Classification Name	Lens, Contact (Other Material) - Daily   More FDA Info for this Device
510(K) Number	K061120
Device Name	Lens, Contact (Other Material) - Daily
Applicant	Synergeyes, Inc. 15825 SHADY GROVE ROAD SUITE 30 ROCKVILLE, MD 20850 US Other 510(k) Applications for this Company
Contact	RICHARD E LIPPMAN, O.D. 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	04/21/2006
Decision Date	06/22/2006
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OP - Ophthalmic
Review Advisory Committee	OP - Ophthalmic
Statement / Summary / Purged Status	Statement
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review