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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 K892741
Device Name PATIENT EXAMINATION GLOVES (LATEX)
Applicant
Dmacs Intl. Corp.
One Perimeter Park S.
Suite 160 N. Tower
Birmingham,  AL  35243
Applicant Contact LESTER W PIOT
Correspondent
Dmacs Intl. Corp.
One Perimeter Park S.
Suite 160 N. Tower
Birmingham,  AL  35243
Correspondent Contact LESTER W PIOT
Regulation Number880.6250
Classification Product Code
LYY  
Date Received04/11/1989
Decision Date 06/09/1989
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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