FDA 510(k) Application Details - K973872

Device Classification Name	Lacrimal Stents And Intubation Sets   More FDA Info for this Device
510(K) Number	K973872
Device Name	Lacrimal Stents And Intubation Sets
Applicant	ATRION MEDICAL PRODUCTS, INC. 1426 CURT FRANCIS RD. ARAB, AL 35016 US Other 510(k) Applications for this Company
Contact	DAN CLARK 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	10/10/1997
Decision Date	01/08/1998
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