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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Table, Physical Therapy, Multi Function
510(k) Number K010252
Device Name MAGNUM
Applicant
Magnum Equipment LLC
7222 W. Melrose Ln.
Oklahoma City,  OK  73127
Applicant Contact MONTE REGAL
Correspondent
Magnum Equipment LLC
7222 W. Melrose Ln.
Oklahoma City,  OK  73127
Correspondent Contact MONTE REGAL
Regulation Number890.5880
Classification Product Code
JFB  
Date Received01/26/2001
Decision Date 04/26/2001
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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