FDA 510(k) Application Details - K990672

Device Classification Name	Lacrimal Stents And Intubation Sets   More FDA Info for this Device
510(K) Number	K990672
Device Name	Lacrimal Stents And Intubation Sets
Applicant	HURRICANE MEDICAL 2331K 63RD AVE. EAST BRADENTON, FL 34203 US Other 510(k) Applications for this Company
Contact	DAVID A CLAPP 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	03/02/1999
Decision Date	05/18/1999
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