FDA 510(k) Application Details - K121971

Device Classification Name	Analyzer, Body Composition   More FDA Info for this Device
510(K) Number	K121971
Device Name	Analyzer, Body Composition
Applicant	ZHONGSHAN TRANSTEK ELECTRONICS CO., LTD. NO. 1 FANGHUA STREET HI-TECH DISTRICT CHENGDU, SICHUAN 610041 CN Other 510(k) Applications for this Company
Contact	LEO WANG 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	07/05/2012
Decision Date	09/27/2012
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review