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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 K891343
Device Name GIGLO PATIENT EXAMINATION GLOVE (LATEX)
Applicant
Giant Glove Industrial Co., Ltd.
42 Sugar Maple Dr.
Roslyn,  NY  11576
Applicant Contact HARRISON FULLER
Correspondent
Giant Glove Industrial Co., Ltd.
42 Sugar Maple Dr.
Roslyn,  NY  11576
Correspondent Contact HARRISON FULLER
Regulation Number880.6250
Classification Product Code
LYY  
Date Received03/10/1989
Decision Date 04/25/1989
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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