FDA 510(k) Application Details - K091415

Device Classification Name	System, Measurement, Blood-Pressure, Non-Invasive   More FDA Info for this Device
510(K) Number	K091415
Device Name	System, Measurement, Blood-Pressure, Non-Invasive
Applicant	TRULY INSTRUMENT CO., LTD. TRULY INDUSTRICAL AREA SHANWEI SHI, GUANG DONG 516600 CN Other 510(k) Applications for this Company
Contact	YANG JIAN-HAO Other 510(k) Applications for this Contact
Regulation Number	870.1130   More FDA Info for this Regulation Number
Classification Product Code	DXN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/13/2009
Decision Date	09/04/2009
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review