510(k) K251854

Device
SteadiSet infusion set
Applicant
Tandem Diabetes Care
510(k) number
K251854
Product code
FPA
Decision
Substantially Equivalent (SESE)
Decision date
2025-08-06
Date received
2025-06-17
Regulation
880.5440
Classification name
Set, Administration, Intravascular
Medical specialty
General Hospital
Review panel
General Hospital
Device class
2
Clearance type
Abbreviated
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Karen Mudd
Address
12400 High Bluff Dr. San Diego CA US 92130 92130

FDA Registration Numbers

Source Documents

510(k) summary PDF

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