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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Apparatus, Suction, Operating-Room, Wall Vacuum Powered
510(k) Number K895859
Device Name CONTAIN(TM)
Applicant
Arbor Technologies, Inc.
3728 Plaza Dr.
Ann Arbor,  MI  48108
Applicant Contact DAWN I MOORE
Correspondent
Arbor Technologies, Inc.
3728 Plaza Dr.
Ann Arbor,  MI  48108
Correspondent Contact DAWN I MOORE
Regulation Number880.6740
Classification Product Code
GCX  
Date Received10/03/1989
Decision Date 02/07/1991
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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