# K231608: Teleport XT Microcatheter

- Pathway: 510(k) (Traditional)
- Applicant: OrbusNeich Medical (Shenzhen) Co., Ltd.
- Decided: Jan 7, 2024 after 219 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: 10 generations back to K001992 (2000). 17 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 19 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K182360: Teleport Microcatheter, Orbusneich Medical Trading, Inc. (2018) Summary page 4.

## Most influential descendants
- K242588: COREPASS Modular Microcatheter (FLEX); COREPASS Modular Microcatheter (CONTROL) (2025), 0 descendants of its own

## Indications for use
The Teleport XT microcatheters are indicated for: supporting and facilitating the placement of guidewires in the coronary and peripheral vasculature. exchanging guidewires in the coronary and peripheral vasculature. the delivery of contrast media into the coronary, peripheral, and abdominal vasculature.

Source page: https://510kreport.com/device/K231608
Methodology: https://510kreport.com/methodology