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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 PLACE
GLEN ROCK,  NJ  07452
Applicant Contact SAUL LISS
Correspondent
MEDICAL CONSULTANTS INTL. LTD.
59 OXFORD PLACE
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
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