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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Set, Administration, Intravascular
510(k) Number K123874
Device Name INTERLINK SYSTEM BURETROL SOLUTION SETS, INTERLINK SYSTEM BURETROL SOLUTION SETS, CONTINUED, CLEARLINK SYSTEM BURETROL S
Applicant
BAXTER HEALTHCARE CORP.
32650 N WILSON RD.
ROUND LAKE,  IL  60073
Applicant Contact NANETTE HEDDEN
Correspondent
BAXTER HEALTHCARE CORP.
32650 N WILSON RD.
ROUND LAKE,  IL  60073
Correspondent Contact NANETTE HEDDEN
Regulation Number880.5440
Classification Product Code
FPA  
Date Received12/17/2012
Decision Date 01/10/2013
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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