FDA 510(k) Application Details - K062482

Device Classification Name	Set, I.V. Fluid Transfer   More FDA Info for this Device
510(K) Number	K062482
Device Name	Set, I.V. Fluid Transfer
Applicant	MEDIMOP MEDICAL PROJECTS, LTD. 17 HAYETZIRA ST. P.O. BOX 2499 RAANANA 43665 IL Other 510(k) Applications for this Company
Contact	ARI Y SOBEL Other 510(k) Applications for this Contact
Regulation Number	880.5440   More FDA Info for this Regulation Number
Classification Product Code	LHI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/24/2006
Decision Date	11/03/2006
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review