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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 K891979
Device Name PATIENT EXAMINATION GLOVE (LATEX)
Applicant
Jeanine Alcantara Intl.
7077 Alvern St., Suite 302
Los Angeles,  CA  90045
Applicant Contact JEANINE ALCANTARA
Correspondent
Jeanine Alcantara Intl.
7077 Alvern St., Suite 302
Los Angeles,  CA  90045
Correspondent Contact JEANINE ALCANTARA
Regulation Number880.6250
Classification Product Code
LYY  
Date Received03/29/1989
Decision Date 04/28/1989
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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