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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name set, blood transfusion
510(k) Number K993120
Device Name MODIFIED BLOOD RECIPIENT SET
Applicant
BAXTER HEALTHCARE CORP.
RT. 120 & WILSON RD.
ROUND LAKE,  IL  60073
Applicant Contact JUDY KANNENBERG
Correspondent
BAXTER HEALTHCARE CORP.
RT. 120 & WILSON RD.
ROUND LAKE,  IL  60073
Correspondent Contact JUDY KANNENBERG
Regulation Number880.5440
Classification Product Code
BRZ  
Date Received09/20/1999
Decision Date 11/17/1999
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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