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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 K892974
Device Name PATIENT EXAMINATION GLOVES
Applicant
Dubo Latex , Ltd.
5250 N. Leamington Ave.
Chicago,  IL  60630
Applicant Contact DUCK S YIM
Correspondent
Dubo Latex , Ltd.
5250 N. Leamington Ave.
Chicago,  IL  60630
Correspondent Contact DUCK S YIM
Regulation Number880.6250
Classification Product Code
LYY  
Date Received04/12/1989
Decision Date 08/17/1989
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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