# K253262: EmeryGlide™ (EG18008901)

- Pathway: 510(k) (Special)
- Applicant: Nano4imaging GmbH
- Decided: Mar 6, 2026 after 158 days
- Product code: DQX (Wire, Guide, Catheter)
- Device class: 2
- Regulation: 21 CFR 870.1330
- 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 K863138 (1986). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K173423: MR Wire Guide Wire Straight, MR Wire Guide Wire Angled, Nano4imaging GmbH (2017) Summary page 5.

## Indications for use
EmeryGlide is intended to direct a catheter to the desired anatomical location in the vasculatory system during diagnostic or interventional procedures.

Source page: https://510kreport.com/device/K253262
Methodology: https://510kreport.com/methodology