# K260771: TruSelect™ 2.6 Microcatheter

- Pathway: 510(k) (Special)
- Applicant: Boston Scientific Corporation
- Decided: May 15, 2026 after 67 days
- Product code: KRA (Catheter, Continuous Flush)
- Device class: 2
- Regulation: 21 CFR 870.1210
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 6 generations back to K000177 (2000). 6 ancestors in all.
No later device cites it as a predicate yet.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K201792: TRUSELECT Microcatheter, Boston Scientific Corporation (2020) Summary page 5.

## Indications for use
The TruSelect 2.6 Microcatheter is intended to provide a conduit for the selective infusion of diagnostic, embolic, or therapeutic agents to target vessels within the peripheral vasculature during endovascular procedures. The microcatheter is coaxially tracked over a steerable guidewire to access the distal peripheral vasculature. Diagnostic, embolic, or therapeutic agents should be used in accordance with specifications outlined by the manufacturer.

Source page: https://510kreport.com/device/K260771
Methodology: https://510kreport.com/methodology