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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Vinyl Patient Examination Glove
510(k) Number K060884
Device Name POWDER-FREE VINYL PATIENT EXAMINATION GLOVES
Applicant
Wei Fang Jiuzhou Gloves Co., Ltd.
209 Bei Si Huan Zhong Rd.,
R. 106 Bldg. 1 Jianxiang Yuan
Beijing, Haidian Distric,  CN
Applicant Contact CHU XIAOAN
Correspondent
Wei Fang Jiuzhou Gloves Co., Ltd.
209 Bei Si Huan Zhong Rd.,
R. 106 Bldg. 1 Jianxiang Yuan
Beijing, Haidian Distric,  CN
Correspondent Contact CHU XIAOAN
Regulation Number880.6250
Classification Product Code
LYZ  
Date Received03/31/2006
Decision Date 05/04/2006
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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