FDA 510(k) Application Details - K020193

Device Classification Name	Lenses, Soft Contact, Daily Wear   More FDA Info for this Device
510(K) Number	K020193
Device Name	Lenses, Soft Contact, Daily Wear
Applicant	CL MCINTOSH 12300 TWINBROOK PKWY. STE. 230 ROCKVILLE, MD 20852 US Other 510(k) Applications for this Company
Contact	RICHARD E LIPPMAN 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	01/18/2002
Decision Date	02/28/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OP - Ophthalmic
Review Advisory Committee	OP - Ophthalmic
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review