FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

Vigilant Software Suite – Vigilant Master Med

K Number: K210075 · Decision Mar 1, 2022
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
9
Applicant Total
12
Review Days
413

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Basic Information

Device Name
Vigilant Software Suite – Vigilant Master Med
K Number
K210075
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5725
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Fresenius Kabi AG
Date Received
January 12, 2021
Decision Date
March 1, 2022
Product Code
PHC
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
PHC Infusion Safety Management Software

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K Number Device Name
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K210074 Agilia SP Infusion System, Agilia SP MC WIFI Infusion Pump, Agilia Link, Agilia Duo, Agilia USB Cable
K210089 CATSmart, Automated Blood Processing Autotransfusion System
K200530 AMICUS Separator System
K192150 AMICUS Separator System
K192368 CATSmart
K180831 CATSmart
K160735 CATSmart
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