FDA 510(k) Application Details - K242115

Device Classification Name Pump, Infusion

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510(K) Number K242115
Device Name Pump, Infusion
Applicant ICU Medical Inc.
600 N. Field Drive
Lake Forest, IL 60045 US
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Contact Yuliya Matlin
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Regulation Number 880.5725

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Classification Product Code FRN
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Date Received 07/19/2024
Decision Date 04/02/2025
Decision SESE - SUBST EQUIV
Classification Advisory Committee HO - General Hospital
Review Advisory Committee HO - General Hospital
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review

FDA Source Information for K242115


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