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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Saliva, Artificial
510(k) Number K810157
Device Name MOI-STIR
Applicant
KINGSWOOD LABORATORIES, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
KINGSWOOD LABORATORIES, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Classification Product Code
LFD  
Date Received01/21/1981
Decision Date 02/10/1981
Decision Substantially Equivalent (SESE)
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
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