FDA 510(k) Application Details - K082182

Device Classification Name	Pump, Infusion   More FDA Info for this Device
510(K) Number	K082182
Device Name	Pump, Infusion
Applicant	Q-CORE, LTD PO BOX 3341 14 HAMEFALSIM ST. KIRYAT ARYEH PETACH TIKVA 49130 IL Other 510(k) Applications for this Company
Contact	ASHER KASSEL Other 510(k) Applications for this Contact
Regulation Number	880.5725   More FDA Info for this Regulation Number
Classification Product Code	FRN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/01/2008
Decision Date	08/15/2008
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	Y
Expedited Review