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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Cement, Dental
510(k) Number K993556
Device Name LIQUIBAND DENTAL
Applicant
Medlogic Global Corp.
4815 List Dr., Suite 111
Colorado Springs,  CO  80919
Applicant Contact STEPHEN J TAMSETT
Correspondent
Medlogic Global Corp.
4815 List Dr., Suite 111
Colorado Springs,  CO  80919
Correspondent Contact STEPHEN J TAMSETT
Regulation Number872.3275
Classification Product Code
EMA  
Date Received10/20/1999
Decision Date 01/03/2000
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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