# K111490: Marksman Catheter, *Refers to Different Catheter Working Lenghts, Distal Single Coiled Lengths and Distal Shaft Lengths

- Pathway: 510(k) (Special)
- Applicant: Ev3, Inc.
- Decided: Sep 16, 2011 after 108 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
No predicates in its family tree.
5 later devices descend from it; 3 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Marksman Catheter: named in the summary without a submission number

## Most influential descendants
- K152625: MMS Guide Catheter (2016), 2 descendants of its own
- K163231: Chameleon PTA Balloon Catheter (2017), 1 descendant of its own
- K170406: Plato MICROCATH 27B Microcatheter (2017), 0 descendants of its own
- K170635: Chameleon PTA Balloon Catheter (2017), 0 descendants of its own
- K143398: Plato MICROCATH 27B Microcatheter (2015), 0 descendants of its own

## Indications for use
The MarksmanTM Catheter is indicated for the introduction of interventional devices and infusion of diagnostic or therapeutic agents into the neuro, peripheral and coronary vasculature.

Source page: https://510kreport.com/device/K111490
Methodology: https://510kreport.com/methodology