# K093050: Arrow Seldinger Arterial Catherization Devices, Models EX Sac 00520

- Pathway: 510(k) (Special)
- Applicant: Arrow Intl., Inc.
- Decided: Dec 18, 2009 after 79 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.
3 later devices descend from it; 1 cites it directly.
2 of 5 devices in its family (counting itself) have 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 1.

## Most influential descendants
- K171146: Arrow Seldinger Arterial Catheterization Device 18 ga., Arrow Seldinger Arterial Catheterization Device 20 ga., Arrow Seldinger Arterial Catheterization Device 22 ga., Arrow Seldinger Arterial Catheterization Device 24 ga. (2017), 2 descendants of its own
- K201726: Arterial Catheter (2021), 0 descendants of its own
- K181563: The ARTERIAL WAND Safety Introducer with Arterial Catheter made of ChronoFlex C with BioGUARD Technology (2018), 0 descendants of its own

## Indications for use
The Arrow® Seldinger Arterial Catheterization Devices permit access to the peripheral arterial circulation or to other small vessels.

Source page: https://510kreport.com/device/K093050
Methodology: https://510kreport.com/methodology