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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 K993222
Device Name INNOVATIVE GLOVES, LATEX EXAMINATION GLOVES POWDERFREE
Applicant
Innovative Gloves Co;, Ltd.
11 Chotevittayakul 3 Rd.
Hatyai, Songkhla,  TH
Applicant Contact RAJEEV KUMAR SOOD
Correspondent
Innovative Gloves Co;, Ltd.
11 Chotevittayakul 3 Rd.
Hatyai, Songkhla,  TH
Correspondent Contact RAJEEV KUMAR SOOD
Regulation Number880.6250
Classification Product Code
LYY  
Date Received09/27/1999
Decision Date 11/05/1999
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Statement Statement
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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