FDA 510(k) Application Details - K042275

Device Classification Name	Lenses, Soft Contact, Daily Wear   More FDA Info for this Device
510(K) Number	K042275
Device Name	Lenses, Soft Contact, Daily Wear
Applicant	VISTAKON 3012 ST. CHARLES DR. TAMPA, FL 33618 US Other 510(k) Applications for this Company
Contact	ANNETTE M HILLRING 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	08/23/2004
Decision Date	10/28/2004
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