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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 K901026
Device Name MJ PERCUSSOR(TM)
Applicant
MERCED MEDICAL, INC.
113300 A-49TH ST. NORTH
CLEARWATER,  FL  34622
Applicant Contact JEFF RATNER
Correspondent
MERCED MEDICAL, INC.
113300 A-49TH ST. NORTH
CLEARWATER,  FL  34622
Correspondent Contact JEFF RATNER
Regulation Number868.5665
Classification Product Code
BYI  
Date Received03/06/1990
Decision Date 03/15/1990
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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