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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Stimulator, Muscle, Powered
510(k) Number K870947
Device Name DYNATRON 500
Applicant
Dynatronics Corp.
C/O King & Spalding
1730 Pennsylvania Ave., NW
Washington,  DC  20006
Applicant Contact JESS H STRIBLING
Correspondent
Dynatronics Corp.
C/O King & Spalding
1730 Pennsylvania Ave., NW
Washington,  DC  20006
Correspondent Contact JESS H STRIBLING
Regulation Number890.5850
Classification Product Code
IPF  
Date Received03/09/1987
Decision Date 08/18/1987
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Physical Medicine
510k Review Panel Physical Medicine
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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