# K151724: AngioDynamics Mariner Angiographic Catheters

- Pathway: 510(k) (Special)
- Applicant: AngioDynamics, Inc.
- Decided: Oct 14, 2015 after 110 days
- Product code: DQO (Catheter, Intravascular, Diagnostic)
- Device class: 2
- Regulation: 21 CFR 870.1200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K112452 (2012). 1 ancestor in all.
2 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K112452: Angiodynamics Soft-VU Angiographic Catheters, AngioDynamics, Inc. (2012) Summary page 4.

## Most influential descendants
- K161596: Soft-Vu, Mariner, Accu-Vu and AngioOptic Catheters (2017), 1 descendant of its own
- K173762: AngioDynamics, Inc. Soft-Vu and Mariner Angiographic Catheters (2018), 0 descendants of its own

## Indications for use
Angiodynamics Angiographic Catheters are for use where angiographic diagnosis is indicated.

Source page: https://510kreport.com/device/K151724
Methodology: https://510kreport.com/methodology