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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 K920890
Device Name OPERATING TABLE SYSTEM-BETAMAQUET 1140
Applicant
STIERLEN-MAQUET AG
KEHLER STRASSE 31
7550 RASTATT
WEST GERMANY,  GR
Applicant Contact BASTERT
Correspondent
STIERLEN-MAQUET AG
KEHLER STRASSE 31
7550 RASTATT
WEST GERMANY,  GR
Correspondent Contact BASTERT
Regulation Number878.4960
Classification Product Code
FQO  
Date Received02/12/1992
Decision Date 07/02/1992
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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