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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Goniometer, Ac-Powered
510(k) Number K897178
Device Name DYNATRON 360 RANGE OF MOTION TESTING DEVICE
Applicant
Dynatronics Corp.
470 Lawndale Dr., Bldg.
D
Salt Lake City,  UT  84115
Applicant Contact H CULLIMORE
Correspondent
Dynatronics Corp.
470 Lawndale Dr., Bldg.
D
Salt Lake City,  UT  84115
Correspondent Contact H CULLIMORE
Regulation Number888.1500
Classification Product Code
KQX  
Date Received12/27/1989
Decision Date 04/18/1990
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Orthopedic
510k Review Panel Neurology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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