FDA 510(k) Application Details - K023796

Device Classification Name	Plethysmograph, Pressure   More FDA Info for this Device
510(K) Number	K023796
Device Name	Plethysmograph, Pressure
Applicant	ERICH JAEGER GMBH 22705 SAVI RANCH PKWY. YORBA LINDA, CA 92887-4645 US Other 510(k) Applications for this Company
Contact	EARL DRAPER Other 510(k) Applications for this Contact
Regulation Number	868.1750   More FDA Info for this Regulation Number
Classification Product Code	CCM Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/13/2002
Decision Date	03/03/2003
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review