Atlas FDA

Agilia VP Infusion System, Agilia VP MC WIFI Infusion Pump, Volumat Lines Administration Sets, Agilia Link, Agilia Duo

FDA 510(k) clearance K210073 · decided 2022-03-01

Clearance details

K-number
K210073
Device name
Agilia VP Infusion System, Agilia VP MC WIFI Infusion Pump, Volumat Lines Administration Sets, Agilia Link, Agilia Duo
Applicant
Fresenius Kabi AG
Decision
Substantially Equivalent
Date received
2021-01-12
Decision date
2022-03-01
Days to decision
413 days
Clearance type
Traditional
Product code
FRN
Device class
2
Regulation number
880.5725
Medical specialty
General Hospital
Advisory committee
General Hospital
Location
Bad Homburg, DE
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.