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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Filter, Conduction, Anesthetic
510(k) Number K902666
Device Name ANESTHESIA CONDUCTION FILTER
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 Number868.5130
Classification Product Code
BSN  
Date Received06/18/1990
Decision Date 04/23/1991
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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