# K160448: Artline

- Pathway: 510(k) (Traditional)
- Applicant: Health Line International Corporation
- Decided: Jul 12, 2016 after 145 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: 1 generation back to K810675 (1981). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
1 of 3 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K810675: Arrow Radial Artery Catheterization Set, Arrow Intl., Inc. (1981) Summary page 5.

## Most influential descendants
- K210548: Medline Integrated Arterial Catheter (2022), 0 descendants of its own

## Indications for use
The ARTLINE Device is intended to permit access to the peripheral arterial circulation system for short term access (less than 30 days).

Source page: https://510kreport.com/device/K160448
Methodology: https://510kreport.com/methodology