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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Table, Operating-Room, Ac-Powered
510(k) Number K926525
Device Name BETASTAR 1131.02 MOBILE OPERATING TABLE
Applicant
Stierlen-Maquet AG
76437 Rastatt
West-Germany,  DE
Applicant Contact PFEUFFER
Correspondent
Stierlen-Maquet AG
76437 Rastatt
West-Germany,  DE
Correspondent Contact PFEUFFER
Regulation Number878.4960
Classification Product Code
FQO  
Subsequent Product Code
GDC  
Date Received12/30/1992
Decision Date 10/12/1993
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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