FDA 510(k) Application Details - K060538

Device Classification Name	Analyzer, Body Composition   More FDA Info for this Device
510(K) Number	K060538
Device Name	Analyzer, Body Composition
Applicant	BEAVERITE INTERNATIONAL LIMITED 5600 WISCONSIN AVE. SUITE 509 CHEVY CHASE, MD 20815 US Other 510(k) Applications for this Company
Contact	PATSY J TRISLER 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	02/28/2006
Decision Date	10/10/2006
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