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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 K893075
Device Name PATIENT EXAMINATION GLOVES
Applicant
Quality Latex Corp. Sdn Bhd
32 Jalan Sungei Besi
57100 Kuala Lumpur
Malaysia,  MY
Applicant Contact WILLIAM CHEONG
Correspondent
Quality Latex Corp. Sdn Bhd
32 Jalan Sungei Besi
57100 Kuala Lumpur
Malaysia,  MY
Correspondent Contact WILLIAM CHEONG
Regulation Number880.6250
Classification Product Code
LYY  
Date Received04/13/1989
Decision Date 11/07/1989
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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