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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Chair, Surgical, Ac-Powered
510(k) Number K831325
Device Name NUTROMAT
Applicant
Medlog GmbH Marketing Services
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Medlog GmbH Marketing Services
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number878.4960
Classification Product Code
GBB  
Date Received04/25/1983
Decision Date 06/02/1983
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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