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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 K874505
Device Name CONTAIN(TM)
Applicant
Arbor Technologies, Inc.
3728-1 Plz. Dr.
Ann Arbor,  MI  48104
Applicant Contact DAWN I MOORE
Correspondent
Arbor Technologies, Inc.
3728-1 Plz. Dr.
Ann Arbor,  MI  48104
Correspondent Contact DAWN I MOORE
Regulation Number880.6740
Classification Product Code
GCX  
Date Received11/02/1987
Decision Date 05/20/1988
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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