FDA 510(k) Application Details - K103166

Device Classification Name	Plethysmograph, Impedance   More FDA Info for this Device
510(K) Number	K103166
Device Name	Plethysmograph, Impedance
Applicant	CHEETAH MEDICAL INC. 12154 DARNESTOWN RD. #236 GAITHERSBURG, MD 20878 US Other 510(k) Applications for this Company
Contact	Rhona Shanker 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	10/27/2010
Decision Date	01/25/2011
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Abbreviated
Reviewed By Third Party	N
Expedited Review