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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
510(k) Number K002679
Device Name 6060 MULTI-THERAPY PUMP, MODEL 2M9832; 6060 EPIDURAL PUMP, MODEL 2L9351
Applicant
Baxter Healthcare Corp
Rt. 120 & Wilson Rd.
Round Lake,  IL  60073
Applicant Contact JENNIFER M PAINE
Correspondent
Baxter Healthcare Corp
Rt. 120 & Wilson Rd.
Round Lake,  IL  60073
Correspondent Contact JENNIFER M PAINE
Regulation Number880.5725
Classification Product Code
FRN  
Date Received08/28/2000
Decision Date 09/18/2000
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
Recalls CDRH Recalls
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