FDA 510(k) Application Details - K020363

Device Classification Name	Latex Patient Examination Glove   More FDA Info for this Device
510(K) Number	K020363
Device Name	Latex Patient Examination Glove
Applicant	GREAT GLOVE SDN BHD 24, JALAN RAJA MOKHTAR DUA KAPAR, SELANGOR D.E. 42200 MY Other 510(k) Applications for this Company
Contact	NOOR AKILAH 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	02/04/2002
Decision Date	04/10/2002
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