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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 K022869
FOIA Releasable 510(k) K022869
Device Name SOAKER CATHETER
Applicant
I-Flow Corp.
20202 Windrow Dr.
Lake Forest,  CA  92630
Applicant Contact SHANE NOEHRE
Correspondent
I-Flow Corp.
20202 Windrow Dr.
Lake Forest,  CA  92630
Correspondent Contact SHANE NOEHRE
Regulation Number880.5725
Classification Product Code
FRN  
Subsequent Product Code
MRZ  
Date Received08/29/2002
Decision Date 09/20/2002
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
Predetermined Change
Control Plan Authorized		 No
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