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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Platform, Force-Measuring
510(k) Number K863443
Device Name DUAL FORCEPLATE
Applicant
Neurocom International, Inc.
2326 NW Lovejoy St.
P.O. Box 12529
Portland,  OR  97210
Applicant Contact JACK KELLY
Correspondent
Neurocom International, Inc.
2326 NW Lovejoy St.
P.O. Box 12529
Portland,  OR  97210
Correspondent Contact JACK KELLY
Regulation Number890.1575
Classification Product Code
KHX  
Date Received09/05/1986
Decision Date 09/17/1986
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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