# K091559: Marksmann Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Chestnut Medical Technologies, Inc.
- Decided: Sep 18, 2009 after 113 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.
14 later devices descend from it; 5 cite it directly.
0 of 15 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 no predicate by number.

## Most influential descendants
- K151638: Phenom 17 Catheter, Phenom 21 Catheter, Phenom 27 Catheter, Phenom Plus Catheter (2015), 6 descendants of its own
- K180959: Phenom 27 Catheter (2018), 4 descendants of its own
- K123477: Via Microcatheter, Via Plus Microcatheter (2013), 4 descendants of its own
- K132652: Via Microcatheter, Via Plus Microcatheter (2013), 3 descendants of its own
- K210230: Phenom Catheters (2021), 2 descendants of its own

## Indications for use
The MarksmanTM Catheter is intended 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/K091559
Methodology: https://510kreport.com/methodology