FDA 510(k) Application Details - K023707

Device Classification Name	Plethysmograph, Photoelectric, Pneumatic Or Hydraulic   More FDA Info for this Device
510(K) Number	K023707
Device Name	Plethysmograph, Photoelectric, Pneumatic Or Hydraulic
Applicant	D. E. HOKANSON, INC. 12840 N.E. 21ST PL. BELLEVUE, WA 98005-1910 US Other 510(k) Applications for this Company
Contact	D. EUGENE HOKANSON 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	11/04/2002
Decision Date	02/12/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review