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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name lamp, surgical, incandescent
510(k) Number K811311
Device Name SKYTRON ELITE SURGICAL TABLES
Applicant
SKYTRON, DIV. THE KMW GROUP, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Correspondent
SKYTRON, DIV. THE KMW GROUP, INC.
803 N. Front St. Suite 3
McHenry,  IL  60050
Regulation Number878.4580
Classification Product Code
GBC  
Date Received05/11/1981
Decision Date 06/02/1981
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
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