# K201792: TRUSELECT Microcatheter

- Pathway: 510(k) (Special)
- Applicant: Boston Scientific Corporation
- Decided: Jul 28, 2020 after 28 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: 5 generations back to K000177 (2000). 5 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K163701: Direxion and Direxion HI-FLO Torqueable Microcatheters, Boston Scientific Corporation (2017) Summary page 5.

## Most influential descendants
- K260771: TruSelect™ 2.6 Microcatheter (2026), 0 descendants of its own

## Indications for use
The TRUSELECTTM Microcatheters are intended for peripheral vascular use. The microcatheter can be used for selective infusion of diagnostic, embolic, or therapeutic materials into the vessel.

Source page: https://510kreport.com/device/K201792
Methodology: https://510kreport.com/methodology