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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 K882010
Device Name POWER EXAMINATION TABLE
Applicant
Enochs Mfg., Inc.
P.O. Box 50199
Indianapolis,  IN  46250
Applicant Contact CHARLES D KELLAM
Correspondent
Enochs Mfg., Inc.
P.O. Box 50199
Indianapolis,  IN  46250
Correspondent Contact CHARLES D KELLAM
Regulation Number878.4960
Classification Product Code
LGX  
Date Received05/13/1988
Decision Date 07/13/1988
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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