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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name table and attachments, operating-room
510(k) Number K873272
Device Name ENDOSCOPY TABLE 1532 ENDOSTAR
Applicant
STIERLEN-MAQUET AG
KEHLER STRASSE 31
7550 RASTATT
WEST GERMANY,  GR
Applicant Contact SCHNELLE
Correspondent
STIERLEN-MAQUET AG
KEHLER STRASSE 31
7550 RASTATT
WEST GERMANY,  GR
Correspondent Contact SCHNELLE
Regulation Number878.4950
Classification Product Code
BWN  
Date Received08/17/1987
Decision Date 09/08/1987
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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