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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 K894967
Device Name LATEX PATIENT EXAMINATION GLOVES
Applicant
Yan Ling Rubber Products Co.
21 Village Sq.
Glen Cove,  NY  11542
Applicant Contact GUO ANSHENG
Correspondent
Yan Ling Rubber Products Co.
21 Village Sq.
Glen Cove,  NY  11542
Correspondent Contact GUO ANSHENG
Regulation Number880.6250
Classification Product Code
LYY  
Date Received08/07/1989
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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