# K173762: AngioDynamics, Inc. Soft-Vu and Mariner Angiographic Catheters

- Pathway: 510(k) (Special)
- Applicant: AngioDynamics, Inc.
- Decided: Jul 18, 2018 after 219 days
- Product code: DQO (Catheter, Intravascular, Diagnostic)
- Device class: 2
- Regulation: 21 CFR 870.1200
- Recalls of this device: 18 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K112452 (2012). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K161596: Soft-Vu, Mariner, Accu-Vu and AngioOptic Catheters, AngioDynamics, Inc. (2017) Summary page 4.

## Recalls of this device
- Mar 3, 2026 · Class II · Z-1861-2026: The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Mar 3, 2026 · Class II · Z-1859-2026: The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Mar 3, 2026 · Class II · Z-1866-2026: The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Mar 3, 2026 · Class II · Z-1864-2026: The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Mar 3, 2026 · Class II · Z-1868-2026: The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Mar 3, 2026 · Class II · Z-1863-2026: The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Mar 3, 2026 · Class II · Z-1867-2026: The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Mar 3, 2026 · Class II · Z-1858-2026: The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Mar 3, 2026 · Class II · Z-1856-2026: The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Mar 3, 2026 · Class II · Z-1871-2026: The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Mar 3, 2026 · Class II · Z-1860-2026: The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Mar 3, 2026 · Class II · Z-1862-2026: The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Mar 3, 2026 · Class II · Z-1869-2026: The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Mar 3, 2026 · Class II · Z-1857-2026: The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Mar 3, 2026 · Class II · Z-1870-2026: The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Mar 3, 2026 · Class II · Z-1865-2026: The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
- Jun 18, 2024 · Class II · Z-2454-2024: Mislabeled. The shelf-box labeling (unit of sale) is accurate for the packaged devices, however the inner pouch label may contain information for a different model (catheter length)
- Jun 18, 2024 · Class II · Z-2453-2024: Mislabeled. The shelf-box labeling (unit of sale) is accurate for the packaged devices, however the inner pouch label may contain information for a different model (catheter length)

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

Source page: https://510kreport.com/device/K173762
Methodology: https://510kreport.com/methodology