FDA 510(k) Application Details - K001677

Device Classification Name	System, Monitoring, Perinatal   More FDA Info for this Device
510(K) Number	K001677
Device Name	System, Monitoring, Perinatal
Applicant	HUNTLEIGH DIAGNOSTICS LTD. 35 PORTMANMOOR ROAD CARDIFF WALES CF2 2HB GB Other 510(k) Applications for this Company
Contact	B. J COLLEYPRIEST 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	06/01/2000
Decision Date	08/14/2000
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OB - Obstetrics/Gynecology
Review Advisory Committee	OB - Obstetrics/Gynecology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review