FDA 510(k) Application Details - K141389

Device Classification Name	Pump, Infusion   More FDA Info for this Device
510(K) Number	K141389
Device Name	Pump, Infusion
Applicant	Q CORE MEDICAL LTD 12154 DARNESTOWN ROAD #236 GAITHERSBURG, MD 20878 US Other 510(k) Applications for this Company
Contact	Rhona Shanker 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	05/27/2014
Decision Date	12/11/2014
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