FDA 510(k) Application Details - K030203

Device Classification Name	Analyzer, Body Composition   More FDA Info for this Device
510(K) Number	K030203
Device Name	Analyzer, Body Composition
Applicant	LONG WELL ELECTRONICS CORP. 3892 SOUTH AMERICA WEST TRAIL FLAGSTAFF, AZ 86001 US Other 510(k) Applications for this Company
Contact	JENNIFER REICH 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	01/21/2003
Decision Date	04/21/2003
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