# K230726: CEREGLIDE 92 Intermediate Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Cerenovus, Inc.
- Decided: Nov 29, 2023 after 258 days
- Product code: QJP (Catheter, Percutaneous, Neurovasculature)
- 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: 9 generations back to K010954 (2001). 14 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 16 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K212224: TracStar LDP Large Distal Platform; Zoom 88 Large Distal Platform, Imperative Care, Inc. (2021) Summary page 4.

## Most influential descendants
- K233982: CEREGLIDE 92 Catheter System (2024), 0 descendants of its own

## Indications for use
The CEREGLIDE 92 Intermediate Catheter is indicated for use in facilitating the insertion and guidance of appropriately sized interventional devices into a selected blood vessel in the neurovascular system.

Source page: https://510kreport.com/device/K230726
Methodology: https://510kreport.com/methodology