FDA 510(k) Application Details - K030353

Device Classification Name	Lacrimal Stents And Intubation Sets   More FDA Info for this Device
510(K) Number	K030353
Device Name	Lacrimal Stents And Intubation Sets
Applicant	EAGLE VISION, INC. 8500 WOLF LAKE DR. SUITE 110 MEMPHIS, TN 38133 US Other 510(k) Applications for this Company
Contact	BILLY HANNAFORD Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	OKS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/03/2003
Decision Date	04/25/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	OP - Ophthalmic
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review