# K171600: Renal Access Cobra Catheter, Kumpe Access Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Cook Incorporated
- Decided: Feb 16, 2018 after 260 days
- Product code: KOD (Catheter, Urological)
- Device class: 2
- Regulation: 21 CFR 876.5130
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K965229 (1997). 3 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K102527: Imager II Urology Torque Catheter (C1 Tip); Imager II Urology Torque Catheter (C2 Tip; Imager II Urology Torque Catheter, Boston Scientific Corporation (2010) Summary page 5.

## Most influential descendants
- K181144: Angled Tip Ureteral Catheter (2018), 0 descendants of its own

## Indications for use
This device is intended for delivery of contrast media as well as access, advancement, or exchange of wire guides in the renal area. These devices are intended for access and catheterization of the urinary tract, including the following applications: Delivery of contrast media Navigation of a tortuous ureter Access, advancement, or exchange of wire guides

Source page: https://510kreport.com/device/K171600
Methodology: https://510kreport.com/methodology