FDA 510(k) Application Details - K071910

Device Classification Name	Polymer Patient Examination Glove   More FDA Info for this Device
510(K) Number	K071910
Device Name	Polymer Patient Examination Glove
Applicant	HARTALEGA SDN BHD # 7, KAWASAN PERUSAHAAN SURIA BATANG BERJUNTAI SELANGOR, DARUL EHSAN 45600 MY Other 510(k) Applications for this Company
Contact	NURUL AISYAH KONG BT ABDULLAH Other 510(k) Applications for this Contact
Regulation Number	880.6250   More FDA Info for this Regulation Number
Classification Product Code	LZA Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	07/11/2007
Decision Date	09/06/2007
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	HO - General Hospital
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review