FDA 510(k) Application Details - K072325

Device Classification Name	Analyzer, Body Composition   More FDA Info for this Device
510(K) Number	K072325
Device Name	Analyzer, Body Composition
Applicant	JAWON MEDICAL CO., LTD. #1208-12, Sinsang-Li, Jinryang-Myun Kyungsan-city, Kyungsan-Bukdo 712-830 KR Other 510(k) Applications for this Company
Contact	Won-Hee Park 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	08/20/2007
Decision Date	11/30/2007
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