FDA 510(k) Application Details - K020909

Device Classification Name	Meter, Conductivity, Non-Remote   More FDA Info for this Device
510(K) Number	K020909
Device Name	Meter, Conductivity, Non-Remote
Applicant	IBP INSTRUMENTS GMBH SUTELSTR. 7A HANNOVER 30659 DE Other 510(k) Applications for this Company
Contact	WERNER PFINGSTMANN Other 510(k) Applications for this Contact
Regulation Number	876.5820   More FDA Info for this Regulation Number
Classification Product Code	FIZ Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	03/20/2002
Decision Date	05/22/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	Y
Expedited Review