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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 K897139
Device Name LATEX PATIENT EXAMINATION GLOVES
Applicant
Kanam Latex Industries Pvt. , Ltd.
Rr 1, Box 448
Raphine,  VA  24472
Applicant Contact F VELDHUYZEN
Correspondent
Kanam Latex Industries Pvt. , Ltd.
Rr 1, Box 448
Raphine,  VA  24472
Correspondent Contact F VELDHUYZEN
Regulation Number880.6250
Classification Product Code
LYY  
Date Received12/27/1989
Decision Date 01/23/1990
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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