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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name pump, infusion, elastomeric
510(k) Number K943664
Device Name INTERMATE XLV ELASTOMERIC INFUSION SYSTEM
Applicant
BAXTER HEALTHCARE CORP.
RTE. 120 AND WILSON RD.
ROUND LAKE,  IL  60073
Applicant Contact PATRICIA S BARSANTI
Correspondent
BAXTER HEALTHCARE CORP.
RTE. 120 AND WILSON RD.
ROUND LAKE,  IL  60073
Correspondent Contact PATRICIA S BARSANTI
Regulation Number880.5725
Classification Product Code
MEB  
Date Received07/28/1994
Decision Date 11/03/1994
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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