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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 K892135
Device Name PATIENT EXAMINATION GLOVES (LATEX)
Applicant
Archer Exports Private , Ltd.
P.O. Box 17789
62, L.B.S. Marg,
Mulund, Bombay 400 080,  IN
Applicant Contact SHARAT CHANDRA
Correspondent
Archer Exports Private , Ltd.
P.O. Box 17789
62, L.B.S. Marg,
Mulund, Bombay 400 080,  IN
Correspondent Contact SHARAT CHANDRA
Regulation Number880.6250
Classification Product Code
LYY  
Date Received04/04/1989
Decision Date 04/27/1989
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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