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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Unit, Suction Operatory
510(k) Number K925367
Device Name A-DEC 7284 CUSPIDOR, CASCADE
Applicant
A-Dec, Inc.
2601 Crestview Dr.
Newberg,  OR  97132 -9257
Applicant Contact PAT RIDENOUR
Correspondent
A-Dec, Inc.
2601 Crestview Dr.
Newberg,  OR  97132 -9257
Correspondent Contact PAT RIDENOUR
Regulation Number872.6640
Classification Product Code
EBR  
Date Received10/21/1992
Decision Date 04/11/1994
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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