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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 K891274
Device Name PATIENT EXAMINATION GLOVE (LATEX)
Applicant
Yue Chuen Co., Ltd.
12e Bank Tower Bldg.
351-353 King'S Rd.
North Point, Hong Kong,  HK
Applicant Contact WING KWONG
Correspondent
Yue Chuen Co., Ltd.
12e Bank Tower Bldg.
351-353 King'S Rd.
North Point, Hong Kong,  HK
Correspondent Contact WING KWONG
Regulation Number880.6250
Classification Product Code
LYY  
Date Received03/09/1989
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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