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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat
510(k) Number K903675
Device Name MAGNETIC RESONANCE THERAPY DEVICE
Applicant
Mrt, Inc.
1118 3rd St., Unit 208
Santa Monica,  CA  90403
Applicant Contact DAVID SALOFF
Correspondent
Mrt, Inc.
1118 3rd St., Unit 208
Santa Monica,  CA  90403
Correspondent Contact DAVID SALOFF
Regulation Number890.5290
Classification Product Code
ILX  
Date Received08/13/1990
Decision Date 01/17/1991
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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