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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 K101840
Device Name POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)
Applicant
Shijiazhuang Sail Plastic Co., Ltd.
Jianxiang Yuan #209 Bei Si Hua
Bldg. 1, Rm.1606
Beijing,  CN 100083
Applicant Contact CHU XIAOAN
Correspondent
Shijiazhuang Sail Plastic Co., Ltd.
Jianxiang Yuan #209 Bei Si Hua
Bldg. 1, Rm.1606
Beijing,  CN 100083
Correspondent Contact CHU XIAOAN
Regulation Number880.6250
Classification Product Code
LYZ  
Date Received07/01/2010
Decision Date 07/16/2010
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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