FDA 510(k) Application Details - K130232

Device Classification Name	System, Measurement, Blood-Pressure, Non-Invasive   More FDA Info for this Device
510(K) Number	K130232
Device Name	System, Measurement, Blood-Pressure, Non-Invasive
Applicant	JINXINBAO ELECTRONIC CO.,LTD ROOM 404, BLDG 7, JINHUICHANG HOMELAND LIUHONGQIAO RD. WENZHOU, ZHEJIANG 325000 CN Other 510(k) Applications for this Company
Contact	HELEN NAN 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	01/29/2013
Decision Date	09/17/2013
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