# K240971: 87 NeuGlide Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Piraeus Medical
- Decided: Dec 6, 2024 after 241 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: 8 generations back to K010954 (2001). 13 ancestors in all.
2 later devices descend from it; 2 cite 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)
- K203764: TracStar Large Distal Platform, ZOOM 88 Large Distal Platform, ZOOM 88-T Large Distal Platform, Imperative Care, Inc. (2021) Summary page 5.

## Most influential descendants
- K262277: 70 NeuGlide Catheter (2026), 0 descendants of its own
- K251044: 93 NeuFlex Catheter (2025), 0 descendants of its own

## Indications for use
The 87 NeuGlide Catheter is indicated for the introduction of interventional devices into the peripheral, coronary, and neuro vasculature.

Source page: https://510kreport.com/device/K240971
Methodology: https://510kreport.com/methodology