FDA 510(k) Application Details - K970631

Device Classification Name	Plug, Punctum   More FDA Info for this Device
510(K) Number	K970631
Device Name	Plug, Punctum
Applicant	ODYSSEY MEDICAL, INC. 1710 SHELBY OAKS DR., SUITE 21 MEMPHIS, TN 38134 US Other 510(k) Applications for this Company
Contact	RAYMOND G WALLACE 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	02/19/1997
Decision Date	04/23/1997
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