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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Airbrush
510(k) Number K002708
Device Name KAVO CORUND HANDPIECE 2013
Applicant
Kavo America
340 E. Main St.
Lake Zurich,  IL  60047
Applicant Contact JOHN WESTERMEIER
Correspondent
Kavo America
340 E. Main St.
Lake Zurich,  IL  60047
Correspondent Contact JOHN WESTERMEIER
Regulation Number872.6080
Classification Product Code
KOJ  
Date Received08/30/2000
Decision Date 11/28/2000
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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