FDA 510(k) Application Details - K131572

Device Classification Name	Electrocardiograph   More FDA Info for this Device
510(K) Number	K131572
Device Name	Electrocardiograph
Applicant	DIMETEK DIGITAL MEDICAL TECHNOLOGIES LTD 3/F-A2, UNIT 8, XING HUA BUILDING, 6TH INDUSTRIAL ROAD, SHEKOU, SHENZHEN CN Other 510(k) Applications for this Company
Contact	JIMMY GUAN Other 510(k) Applications for this Contact
Regulation Number	870.2340   More FDA Info for this Regulation Number
Classification Product Code	DPS Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/31/2013
Decision Date	07/22/2013
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	Y
Expedited Review