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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Device, Electrical Dental Anesthesia
510(k) Number K900731
Device Name MEDI LISS DENTAL ANALGESIA DEVICE (SBL601)
Applicant
Medical Consultants Intl. , Ltd.
59 Oxford Pl.
Glen Rock,  NJ  07452
Applicant Contact SAUL LISS
Correspondent
Medical Consultants Intl. , Ltd.
59 Oxford Pl.
Glen Rock,  NJ  07452
Correspondent Contact SAUL LISS
Classification Product Code
LWM  
Date Received02/15/1990
Decision Date 12/17/1990
Decision Substantially Equivalent (SESE)
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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