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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name percussor, powered-electric
510(k) Number K936121
Device Name THAIRAPY SYSTEM
Applicant
AMERICAN BIOSYSTEMS, INC.
SUITE 116
ST. PAUL,  MN  55110
Applicant Contact PHILIP R ROSE
Correspondent
AMERICAN BIOSYSTEMS, INC.
SUITE 116
ST. PAUL,  MN  55110
Correspondent Contact PHILIP R ROSE
Regulation Number868.5665
Classification Product Code
BYI  
Date Received12/23/1993
Decision Date 08/02/1994
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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