FDA 510(k) Application Details - K993938

Device Classification Name	System, Measurement, Blood-Pressure, Non-Invasive   More FDA Info for this Device
510(K) Number	K993938
Device Name	System, Measurement, Blood-Pressure, Non-Invasive
Applicant	HOMMED LLC. 19275 WEST CAPITOL DR. SUITE 200 BROOKFIELD, WI 53045 US Other 510(k) Applications for this Company
Contact	HERSCHEL PEDDICORD 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	11/19/1999
Decision Date	03/15/2000
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