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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name circuit, breathing (w connector, adaptor, y piece)
510(k) Number K833871
Device Name UNIVERSAL CONTROL ARM
Applicant
ANESTHESIA ASSOC., INC.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
ANESTHESIA ASSOC., INC.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number868.5240
Classification Product Code
CAI  
Date Received11/08/1983
Decision Date 12/27/1983
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
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