510(k) K210075

Device
Vigilant Software Suite – Vigilant Master Med
Applicant
Fresenius Kabi AG
510(k) number
K210075
Product code
PHC  
Decision
Substantially Equivalent (SESE)
Decision date
2022-03-01
Date received
2021-01-12
Regulation
880.5725
Classification name
Infusion Safety Management Software
Medical specialty
General Hospital
Review panel
General Hospital
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Keith Dunn
Address
Else-Kroner-Str. 1 Bad Homburg DE 61346 61346

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code PHC  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K252130LifeShield Infusion Safety Software SuiteIcu Medical, Inc.2026-04-02
K243062BD Intelliport System; BD Intelliport Reader (516230); BD Intelliport Sensor (516229); BD Intelliport Gateway (516232); BD Intelliport Mount (516233); BD Intelliport Charger (516231)Becton Dickinson2025-06-20
K242117LifeShield Infusion Safety Software SuiteIcu Medical, Inc.2025-04-02
K230665Dose IQ Safety SoftwareBaxter Healthcare Corporation2024-03-29
K223606LifeShield™ Infusion Safety Software SuiteIcu Medical, Inc.2023-08-24
K211124Dose IQ Safety SoftwareBaxter Healthcare Corporation2022-08-30
K182092BD Intelliport SystemBecton, Dickinson and Company2019-04-30
K141474BECTON DICKINSON INTELLIPORT SYSTEMBecton, Dickinson & CO2014-12-18
K141193MEDFUSION 4000 PUMP DEVICE SPECIFIC REPORTS SOLFWARE FOR PHARMGUARD SERVER VERSION 2.0Smiths Medical Asd, Inc.2014-07-25

Legacy Summary#

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FDA Review#

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