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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 K901749
Device Name TABA PATIENT EXAMINATION GLOVES
Applicant
R.S.T. Corp.
P.O. Box 1132
Ballwin,  MO  63022
Applicant Contact THOMAS LAWRENCE
Correspondent
R.S.T. Corp.
P.O. Box 1132
Ballwin,  MO  63022
Correspondent Contact THOMAS LAWRENCE
Regulation Number880.6250
Classification Product Code
LYY  
Date Received04/17/1990
Decision Date 05/30/1990
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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