FDA 510(k) Application Details - K991624

Device Classification Name	Latex Patient Examination Glove   More FDA Info for this Device
510(K) Number	K991624
Device Name	Latex Patient Examination Glove
Applicant	SMART GLOVE CORP. SDN BHD LOT 6487 BATU 5 3/4 SEMENTA, JALAN KAPAR SELANGOR DARUL EHSAN 42100 MY Other 510(k) Applications for this Company
Contact	FOO KHON PU Other 510(k) Applications for this Contact
Regulation Number	880.6250   More FDA Info for this Regulation Number
Classification Product Code	LYY Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/11/1999
Decision Date	07/09/1999
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