FDA 510(k) Application Details - K093192

Device Classification Name	Plethysmograph, Photoelectric, Pneumatic Or Hydraulic   More FDA Info for this Device
510(K) Number	K093192
Device Name	Plethysmograph, Photoelectric, Pneumatic Or Hydraulic
Applicant	ADVANCED VASCULAR DYNAMICS 1910 NW 23RD PLACE PORTLAND, OR 97210 US Other 510(k) Applications for this Company
Contact	HERBERT SEMLER Other 510(k) Applications for this Contact
Regulation Number	870.2780   More FDA Info for this Regulation Number
Classification Product Code	JOM Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/09/2009
Decision Date	02/12/2010
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