FDA 510(k) Application Details - K091855

Device Classification Name	Pump, Infusion   More FDA Info for this Device
510(K) Number	K091855
Device Name	Pump, Infusion
Applicant	BELMONT INSTRUMENT CORP. 780 BOSTON RD. BILLERICA, MA 01821 US Other 510(k) Applications for this Company
Contact	URAIWAN LABADINI 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	06/23/2009
Decision Date	07/01/2009
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Special
Reviewed By Third Party	N
Expedited Review