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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 K051924
Device Name POWDERED VINYL PATIENT EXAMINATION GLOVES, COLORED (WHITE, YELLOW)
Applicant
Shijiazhuang Manful Light Industrial Products Co.,
Rm.1606, Bldg. 1 Jianxiang Yuan
No 209 Bie Si Huan Zhong Rd.
Haidian District, Beijing,  CN 100083
Applicant Contact CHU XIAOAN
Correspondent
Shijiazhuang Manful Light Industrial Products Co.,
Rm.1606, Bldg. 1 Jianxiang Yuan
No 209 Bie Si Huan Zhong Rd.
Haidian District, Beijing,  CN 100083
Correspondent Contact CHU XIAOAN
Regulation Number880.6250
Classification Product Code
LYZ  
Date Received07/15/2005
Decision Date 09/02/2005
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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