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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Table, Examination, Medical, Powered
510(k) Number K894144
Device Name POWER EXAMINATION TABLE MODEL # 405
Applicant
Midmark Corp.
60 Vista Dr.
P.O. Box 286
Versailles,  OH  45380
Applicant Contact JOHN OLDIGES
Correspondent
Midmark Corp.
60 Vista Dr.
P.O. Box 286
Versailles,  OH  45380
Correspondent Contact JOHN OLDIGES
Regulation Number878.4960
Classification Product Code
LGX  
Date Received06/13/1989
Decision Date 08/28/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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