FDA 510(k) Application Details - K031944

Device Classification Name	Polymer Patient Examination Glove   More FDA Info for this Device
510(K) Number	K031944
Device Name	Polymer Patient Examination Glove
Applicant	ARISTA LATINDO INDUSTRIAL, LTD. P.T. JL: K.H.MOH MANSYUR NO. 128 JAKARTA 11210 ID Other 510(k) Applications for this Company
Contact	LINGA SUMARTA 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	06/24/2003
Decision Date	09/23/2003
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