FDA 510(k) Application Details - K001629

Device Classification Name	Pump, Infusion   More FDA Info for this Device
510(K) Number	K001629
Device Name	Pump, Infusion
Applicant	DISETRONIC MEDICAL SYSTEMS AG 7690 CAMERON CIRCLE FORT MYERS, FL 33912 US Other 510(k) Applications for this Company
Contact	Lee Leichter 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	05/26/2000
Decision Date	06/21/2000
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review