FDA 510(k) Application Details - K983838

Device Classification Name	Pump, Infusion   More FDA Info for this Device
510(K) Number	K983838
Device Name	Pump, Infusion
Applicant	ABBOTT LABORATORIES DEPT. 389, AP30 ABBOTT PARK, IL 60064-3537 US Other 510(k) Applications for this Company
Contact	JERRY JENNINGS 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	10/21/1998
Decision Date	11/20/1998
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review