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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Vinyl Patient Examination Glove
510(k) Number K023753
Device Name VINYL EXAMINATION GLOVES, PRE-POWDERED WITH VITAMIN E
Applicant
Arista Latindo Industrial Ltd. P.T
Jl K. H. Moh Mansyur # 128
Jakarta,  ID 11210
Applicant Contact LINGA SUMARTA
Correspondent
Arista Latindo Industrial Ltd. P.T
Jl K. H. Moh Mansyur # 128
Jakarta,  ID 11210
Correspondent Contact LINGA SUMARTA
Regulation Number880.6250
Classification Product Code
LYZ  
Date Received11/08/2002
Decision Date 03/25/2003
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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