510(k) K221327

Device
BD Alaris? Pump Infusion Sets
Applicant
Care Fusion
510(k) number
K221327
Product code
FPA
Decision
Substantially Equivalent (SESE)
Decision date
2023-07-21
Date received
2022-05-06
Regulation
880.5440
Classification name
Set, Administration, Intravascular
Medical specialty
General Hospital
Review panel
General Hospital
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Roya Borazjani
Address
10020 Pacific Mesa Blvd. San Diego CA US 92121 92121

FDA Registration Numbers

Source Documents

510(k) summary PDF

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