Atlas FDA

LifeShield™ Infusion Safety Software Suite

FDA 510(k) clearance K223606 · decided 2023-08-24

Clearance details

K-number
K223606
Device name
LifeShield™ Infusion Safety Software Suite
Applicant
Icu Medical, Inc.
Decision
Substantially Equivalent
Date received
2022-12-02
Decision date
2023-08-24
Days to decision
265 days
Clearance type
Traditional
Product code
PHC
Device class
2
Regulation number
880.5725
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Lake Forest, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
LifeShield Infusion Safety Software Suite (K252130)Icu Medical, Inc.2026-04-02
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Vigilant Software Suite – Vigilant Master Med (K210075)Fresenius Kabi AG2022-03-01
BD Intelliport System (K182092)Becton, Dickinson and Company2019-04-30
BECTON DICKINSON INTELLIPORT SYSTEM (K141474)Becton, Dickinson & CO2014-12-18
MEDFUSION 4000 PUMP DEVICE SPECIFIC REPORTS SOLFWARE FOR PHARMGUARD SERVER VERSION 2.0 (K141193)Smiths Medical Asd, Inc.2014-07-25

Recalls involving this device

RecordFirmDate
LifeShield Drug Library Management (DLM), LifeShield Infusion Safety Software SUite v2.1 a recall (Z-1763-2025)ICU Medical, Inc.2025-05-14