FDA 510(k) Application Details - K955366

Device Classification Name	Lens, Contact (Other Material) - Daily   More FDA Info for this Device
510(K) Number	K955366
Device Name	Lens, Contact (Other Material) - Daily
Applicant	RAND SCIENTIFIC CORP. 4135 NORTHGATE BLVD., SUITE 9 SACRAMENTO, CA 95834 US Other 510(k) Applications for this Company
Contact	DUANE TRACY 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	11/22/1995
Decision Date	03/28/1996
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