FDA 510(k) Application Details - K050826

Device Classification Name	System, Monitoring, Perinatal   More FDA Info for this Device
510(K) Number	K050826
Device Name	System, Monitoring, Perinatal
Applicant	CETRO AMERICA 925 SHERMAN AVENUE HAMDEN, CT 06514 US Other 510(k) Applications for this Company
Contact	MAYA CIANCIOLO Other 510(k) Applications for this Contact
Regulation Number	884.2740   More FDA Info for this Regulation Number
Classification Product Code	HGM Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/01/2005
Decision Date	04/10/2006
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OB - Obstetrics/Gynecology
Review Advisory Committee	OB - Obstetrics/Gynecology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review