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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Apparatus, Vestibular Analysis
510(k) Number K891008
Device Name VESTIBULAR OCULAR REFLEX TEST EQUIPMENT(VORTEQ)
Applicant
Micromedical Technologies, Inc.
110 W. Walnut
Chatham,  IL  62629
Applicant Contact RICHARD MILES, PH.D.
Correspondent
Micromedical Technologies, Inc.
110 W. Walnut
Chatham,  IL  62629
Correspondent Contact RICHARD MILES, PH.D.
Classification Product Code
LXV  
Date Received03/03/1989
Decision Date 05/31/1989
Decision Substantially Equivalent (SESE)
510k Review Panel Ear Nose & Throat
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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