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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 K892095
Device Name PATIENT EXAMINATION GLOVES (LATEX)
Applicant
Madafair , Ltd.
Rm. A. 10/F., Sang Woo Bldg.
227-228 Glouester Rd.
Wanchai, Hong Kong,  HK
Applicant Contact C. F CHEUNG
Correspondent
Madafair , Ltd.
Rm. A. 10/F., Sang Woo Bldg.
227-228 Glouester Rd.
Wanchai, Hong Kong,  HK
Correspondent Contact C. F CHEUNG
Regulation Number880.6250
Classification Product Code
LYY  
Date Received04/03/1989
Decision Date 09/15/1989
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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