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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Latex Patient Examination Glove
510(k) Number K891510
Device Name ARG LATEX EXAMINATION GLOVES
Applicant
Palmbase Rubber Mfg. (M) Sdn Bhd
Lot 8, Jalan P/1a, Bangi Indus
Estate, 43000 Kajang
Selangor Darul Ehsan. W,  MY
Applicant Contact LEONG KIEW
Correspondent
Palmbase Rubber Mfg. (M) Sdn Bhd
Lot 8, Jalan P/1a, Bangi Indus
Estate, 43000 Kajang
Selangor Darul Ehsan. W,  MY
Correspondent Contact LEONG KIEW
Regulation Number880.6250
Classification Product Code
LYY  
Date Received03/16/1989
Decision Date 04/28/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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