FDA 510(k) Application Details - K152659

Device Classification Name	System, Measurement, Blood-Pressure, Non-Invasive   More FDA Info for this Device
510(K) Number	K152659
Device Name	System, Measurement, Blood-Pressure, Non-Invasive
Applicant	MEDIANA CO., LTD 132, DONGHWAGONGDAN-RO, MUNMAK-EUP WONJU-SI 220-801 KR Other 510(k) Applications for this Company
Contact	KIM MIN HYE 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	09/17/2015
Decision Date	08/25/2016
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review