FDA 510(k) Application Details - K991130

Device Classification Name	Plug, Punctum   More FDA Info for this Device
510(K) Number	K991130
Device Name	Plug, Punctum
Applicant	EAGLE VISION, INC. 6263 POPLAR AVENUE, SUITE 650 MEMPHIS, TN 38119 US Other 510(k) Applications for this Company
Contact	JIM BARLEY Other 510(k) Applications for this Contact
Regulation Number	000.0000   More FDA Info for this Regulation Number
Classification Product Code	LZU Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/02/1999
Decision Date	04/20/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	-
Review Advisory Committee	OP - Ophthalmic
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review