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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 K801982
Device Name THE MCSHIRLEY PERCUSSOR
Applicant
MCSHIRLEY PRODUCTS, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
MCSHIRLEY PRODUCTS, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number868.5665
Classification Product Code
BYI  
Date Received08/19/1980
Decision Date 09/16/1980
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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