FDA 510(k) Application Details - K014009

Device Classification Name	Analyzer, Body Composition   More FDA Info for this Device
510(K) Number	K014009
Device Name	Analyzer, Body Composition
Applicant	TANITA CORP. OF AMERICA 2625 SOUTH CLEARBROOK DR. ARLINGTON HGTS., IL 60005 US Other 510(k) Applications for this Company
Contact	CAROL ALLOIAN (BENSON) Other 510(k) Applications for this Contact
Regulation Number	870.2770   More FDA Info for this Regulation Number
Classification Product Code	MNW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/05/2001
Decision Date	06/24/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review