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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 K890872
Device Name PATIENT EXAMINATION GLOVES
Applicant
Unigloves , Ltd.
71 Sap Rd., Sipraya,Bangrak
Bangkok 10500
Thailand,  TH
Applicant Contact ASHOK MUKHERJEE
Correspondent
Unigloves , Ltd.
71 Sap Rd., Sipraya,Bangrak
Bangkok 10500
Thailand,  TH
Correspondent Contact ASHOK MUKHERJEE
Regulation Number880.6250
Classification Product Code
LYY  
Date Received02/24/1989
Decision Date 05/04/1989
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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