# K182360: Teleport Microcatheter

- Pathway: 510(k) (Traditional)
- Applicant: Orbusneich Medical Trading, Inc.
- Decided: Nov 9, 2018 after 71 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: 9 generations back to K001992 (2000). 16 ancestors in all.
2 later devices descend 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)
- K161126: ASAHI Corsair Pro, Asahi Intecc Co., Ltd. (2016) Summary page 4.

## Most influential descendants
- K231608: Teleport XT Microcatheter (2024), 1 descendant of its own
- K242588: COREPASS Modular Microcatheter (FLEX); COREPASS Modular Microcatheter (CONTROL) (2025), 0 descendants of its own

## Indications for use
The Teleport 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/K182360
Methodology: https://510kreport.com/methodology