FDA 510(k) Application Details - K024289

Device Classification Name	Products, Contact Lens Care, Rigid Gas Permeable   More FDA Info for this Device
510(K) Number	K024289
Device Name	Products, Contact Lens Care, Rigid Gas Permeable
Applicant	BAUSCH & LOMB INCORPORATED 1400 N GOODMAN ST. ROCHESTER, NY 14609 US Other 510(k) Applications for this Company
Contact	JENNIFER B MURRAY Other 510(k) Applications for this Contact
Regulation Number	886.5918   More FDA Info for this Regulation Number
Classification Product Code	MRC Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/23/2002
Decision Date	05/02/2003
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