FDA 510(k) Application Details - K072662

Device Classification Name	Plethysmograph, Impedance   More FDA Info for this Device
510(K) Number	K072662
Device Name	Plethysmograph, Impedance
Applicant	CHEETAH MEDICAL INC. INDUSTRIAL PARK 13 MIZPE AVIV, M.P. MISGAV 20187 IL Other 510(k) Applications for this Company
Contact	BENNY ARAZY Other 510(k) Applications for this Contact
Regulation Number	870.2770   More FDA Info for this Regulation Number
Classification Product Code	DSB Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/21/2007
Decision Date	01/16/2008
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