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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 K915717
Device Name CEDETA
Applicant
D-W Intl.
3212 SE 147th Pl.
Suite 103
Vancouver,  WA  98684
Applicant Contact CHARLES R WHITLOCK
Correspondent
D-W Intl.
3212 SE 147th Pl.
Suite 103
Vancouver,  WA  98684
Correspondent Contact CHARLES R WHITLOCK
Classification Product Code
LWM  
Date Received12/19/1991
Decision Date 11/23/1992
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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