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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 K953590
Device Name COMFIT
Applicant
WEMBLEY RUBBER PRODUCTS (M) SDN BHD
LOT 1, JALAN 3,
KAWASAN PERUSAHAAN BANDAR BARU
SALAK TINGGI, SEPANG SELANGOR,  MY 43900
Applicant Contact ONG GHEE CHEE
Correspondent
WEMBLEY RUBBER PRODUCTS (M) SDN BHD
LOT 1, JALAN 3,
KAWASAN PERUSAHAAN BANDAR BARU
SALAK TINGGI, SEPANG SELANGOR,  MY 43900
Correspondent Contact ONG GHEE CHEE
Regulation Number880.6250
Classification Product Code
LYY  
Date Received07/31/1995
Decision Date 06/27/1996
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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