# K170743: AngioDynamics Total Abscession Biliary Drainage Catheter

- Pathway: 510(k) (Special)
- Applicant: AngioDynamics, Inc.
- Decided: Mar 30, 2017 after 20 days
- Product code: FGE (Stents, Drains And Dilators For The Biliary Ducts)
- Device class: 2
- Regulation: 21 CFR 876.5010
- 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 K060023 (2006). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K060023: Angiodynamics Total Abscession Biliary Drainage Catheter, AngioDynamics, Inc. (2006) Summary page 4.

## Indications for use
AngioDynamics Total Abscession Biliary Drainage Catheter is indicated for percutaneous transhepatic biliary drainage.

Source page: https://510kreport.com/device/K170743
Methodology: https://510kreport.com/methodology