# K251745: Welch Allyn FlexiPort Blood Pressure Cuffs (FlexiPort Blood Pressure Cuffs)

- Pathway: 510(k) (Traditional)
- Applicant: Baxter Healthcare Corporation
- Decided: Dec 16, 2025 after 193 days
- Product code: DXQ (Blood Pressure Cuff)
- Device class: 2
- Regulation: 21 CFR 870.1120
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K790810 (1979). 8 ancestors in all.
No later device cites it as a predicate yet.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070060: Welch Allyn Flexiport Disposable Blood Pressure Cuff (One-Piece); Reusable Blood Pressure Cuff (One-Piece), Welch Allyn, Inc. (2007) Summary page 5.

## Indications for use
Welch Allyn FlexiPort Blood Pressure Cuffs are intended to be used for patient health screening assessment to determine patient’s systolic/diastolic blood pressure when used in conjunction with non-automated and automated sphygmomanometers.

Source page: https://510kreport.com/device/K251745
Methodology: https://510kreport.com/methodology