# K152202: Intermediate Catheter, 105 cm, Intermediate Catheter, 115cm, Intermediate Catheter , 125cm

- Pathway: 510(k) (Traditional)
- Applicant: Tni Manufacturing, Inc.
- Decided: Dec 14, 2015 after 130 days
- Product code: DQY (Catheter, Percutaneous)
- Device class: 2
- Regulation: 21 CFR 870.1250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K010954 (2001). 17 ancestors in all.
3 later devices descend from it; 2 cite it directly.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K122772: Penumbra DDC Catheters, Penumbra, Inc. (2012) Summary page 5.

## Most influential descendants
- K171672: 065 Zenith, 074 Zenith (2017), 1 descendant of its own
- K173709: Zenith Support, 95 cm, Zenith Support, 105 cm, Zenith Support, 115 cm (2018), 0 descendants of its own
- K161262: Super Distal Access (SDA) (2016), 0 descendants of its own

## Indications for use
The Intermediate Catheter is indicated for the introduction of interventional devices into the peripheral and neuro vasculature.

Source page: https://510kreport.com/device/K152202
Methodology: https://510kreport.com/methodology