Plum Duo Precision IV Pump
K-Number: K242115 · 2025-04-02
ApplicantIcu Medical, Inc.
Decision Date2025-04-02
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Plum Duo Precision IV Pump is a medical device manufactured by Icu Medical, Inc.. It received FDA 510(k) clearance on 2025-04-02 under approval number K242115. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Plum Duo Precision IV Pump?
Plum Duo Precision IV Pump is a medical device that received FDA 510(k) clearance on 2025-04-02. It is manufactured by Icu Medical, Inc.. The 510(k) number is K242115.
When was Plum Duo Precision IV Pump approved by the FDA?
Plum Duo Precision IV Pump received FDA 510(k) clearance on 2025-04-02, under approval number K242115.
What company makes Plum Duo Precision IV Pump?
Plum Duo Precision IV Pump is manufactured by Icu Medical, Inc..
What is the FDA product code for Plum Duo Precision IV Pump?
The FDA product code for Plum Duo Precision IV Pump is FRN.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.