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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 K891787
Device Name PATIENT EXAMINATION GLOVES (LATEX)
Applicant
Socoil Latex Products Sdn Bhd
167, Jalan Kem
42000 Port Klang
Selangor, Malaysia,  MY
Applicant Contact FRANCIS KHOO
Correspondent
Socoil Latex Products Sdn Bhd
167, Jalan Kem
42000 Port Klang
Selangor, Malaysia,  MY
Correspondent Contact FRANCIS KHOO
Regulation Number880.6250
Classification Product Code
LYY  
Date Received03/23/1989
Decision Date 07/31/1989
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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