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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 K944750
Device Name CORFLO 300 PUMP
Applicant
CORPAK, INC.
100 CHADDICK DR.
WHEELING,  IL  60090
Applicant Contact GEORGE NASSIF
Correspondent
CORPAK, INC.
100 CHADDICK DR.
WHEELING,  IL  60090
Correspondent Contact GEORGE NASSIF
Regulation Number880.5725
Classification Product Code
FRN  
Date Received09/26/1994
Decision Date 06/19/1995
Decision SE SUBJECT TO TRAKING & PMS (PT)
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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