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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Table, Mechanical
510(k) Number K931635
Device Name TREATMENT TABLES, MANUALLY ACTIVATED
Applicant
Med Mart, Inc.
215 12th Ave., NE
Valley City,  ND  58072
Applicant Contact DAVID KESLER
Correspondent
Med Mart, Inc.
215 12th Ave., NE
Valley City,  ND  58072
Correspondent Contact DAVID KESLER
Regulation Number890.3750
Classification Product Code
INW  
Date Received04/01/1993
Decision Date 07/21/1993
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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