FDA 510(k) Application Details - K001898

Device Classification Name	System, Measurement, Blood-Pressure, Non-Invasive   More FDA Info for this Device
510(K) Number	K001898
Device Name	System, Measurement, Blood-Pressure, Non-Invasive
Applicant	MEDWAVE, INC. 4382 ROUND LAKE RD. WEST ARDEN HILLS, MN 55112-3923 US Other 510(k) Applications for this Company
Contact	DONNA R LUNAK 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	06/22/2000
Decision Date	08/31/2000
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