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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 K812803
Device Name INFANT PERCUSSOR #5534
Applicant
HUDSON OXYGEN THERAPY SALES CO.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
HUDSON OXYGEN THERAPY SALES CO.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number868.5665
Classification Product Code
BYI  
Date Received10/06/1981
Decision Date 12/03/1981
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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