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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 K063645
Device Name FREQUENCER, MODEL 1001
Applicant
DYMEDSO INC.
127 MAIN ST.
SPRINGFIELD,  VT  05156
Applicant Contact Jean Bigoney
Correspondent
DYMEDSO INC.
127 MAIN ST.
SPRINGFIELD,  VT  05156
Correspondent Contact Jean Bigoney
Regulation Number868.5665
Classification Product Code
BYI  
Date Received12/07/2006
Decision Date 03/15/2007
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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