510(k) K242339

Device
Intravascular Extension Sets and Accessories
Applicant
Baxter Healthcare Corporation
510(k) number
K242339
Product code
FPA
Decision
Substantially Equivalent (SESE)
Decision date
2025-02-28
Date received
2024-08-07
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
N

Related Records

Applicant Contact

Contact
Bernhard Bartmer
Address
25212 W. Il Rte. 120 Round Lake IL US 60073 60073

FDA Registration Numbers

Source Documents

510(k) summary PDF

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