FDA 510(k) Application Details - K020584

Device Classification Name	System, Measurement, Blood-Pressure, Non-Invasive   More FDA Info for this Device
510(K) Number	K020584
Device Name	System, Measurement, Blood-Pressure, Non-Invasive
Applicant	NEPTEC DESIGN GROUP, LTD. 103 NOLEN LN. CHAPEL HILL, NC 27516 US Other 510(k) Applications for this Company
Contact	CHARLES H KYPER 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	02/21/2002
Decision Date	05/22/2002
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