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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 K883899
Device Name MANUAL PERCUSSOR CUPS
Applicant
MEDICAL COMPONENTS, INC.
411 FREMONT ST.
ANOKA,  MN  55303
Applicant Contact DUNCAN G JOHNSON
Correspondent
MEDICAL COMPONENTS, INC.
411 FREMONT ST.
ANOKA,  MN  55303
Correspondent Contact DUNCAN G JOHNSON
Regulation Number868.5665
Classification Product Code
BYI  
Date Received09/15/1988
Decision Date 12/13/1988
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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