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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name accessories, catheter
510(k) Number K760383
Device Name STOPCOCKS
Original Applicant
B. BRAUN INSTRUMENTS
Regulation Number878.4200
Classification Product Code
KGZ  
Date Received08/05/1976
Decision Date 11/02/1976
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
Recalls CDRH Recalls
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