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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 K891632
Device Name PATIENT EXAMINATION GLOVES (LATEX)
Applicant
Rank Rubber Industries Sdn Bhd
23a Wisma Rank, Jalan Barat
Off Jalan Tmbi 55100
Kuala Lumpur, Malaysia,  MY
Applicant Contact FONG, KAN
Correspondent
Rank Rubber Industries Sdn Bhd
23a Wisma Rank, Jalan Barat
Off Jalan Tmbi 55100
Kuala Lumpur, Malaysia,  MY
Correspondent Contact FONG, KAN
Regulation Number880.6250
Classification Product Code
LYY  
Date Received03/17/1989
Decision Date 04/13/1989
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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