FDA 510(k) Application Details - K022128

Device Classification Name	Lens, Contact (Other Material) - Daily   More FDA Info for this Device
510(K) Number	K022128
Device Name	Lens, Contact (Other Material) - Daily
Applicant	BAUSCH & LOMB INCORPORATED 1400 NORTH GOODMAN ST. ROCHESTER, NY 14609 US Other 510(k) Applications for this Company
Contact	DEBRA L KETCHUM 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	07/01/2002
Decision Date	08/22/2002
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