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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 K891368
Device Name PATIENT EXAMINATION GLOVES (LATEX)
Applicant
Zest Mark Industrial Co., Ltd.
P.O. Box 84-323
Taipei
Taiwan, Roc,  TW
Applicant Contact THOMAS CHEN
Correspondent
Zest Mark Industrial Co., Ltd.
P.O. Box 84-323
Taipei
Taiwan, Roc,  TW
Correspondent Contact THOMAS CHEN
Regulation Number880.6250
Classification Product Code
LYY  
Date Received03/09/1989
Decision Date 03/31/1989
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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