FDA 510(k) Application Details - K984223

Device Classification Name	System, Measurement, Blood-Pressure, Non-Invasive   More FDA Info for this Device
510(K) Number	K984223
Device Name	System, Measurement, Blood-Pressure, Non-Invasive
Applicant	CITIZEN WATCH CO., LTD. 3000 K STREET, N.W., SUITE 500 WASHINGTON, DC 20007 US Other 510(k) Applications for this Company
Contact	JOSEPH D EDMONDSON JR 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	11/25/1998
Decision Date	04/28/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review