FDA 510(k) Application Details - K000485

Device Classification Name	Lens, Contact (Other Material) - Daily   More FDA Info for this Device
510(K) Number	K000485
Device Name	Lens, Contact (Other Material) - Daily
Applicant	INNOVISION, INC. 3125 SOUTH 61ST AVE. OMAHA, NE 68106-3675 US Other 510(k) Applications for this Company
Contact	DON M WOODFORD 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	02/14/2000
Decision Date	05/12/2000
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