# DEN080009: Airpurge

- Pathway: De Novo (Post-NSE)
- Applicant: Anesthesia Safety Products, LLC
- Decided: Mar 4, 2014 after 1,952 days
- Product code: OKL (Intravascular Administration Set, Automated Air Removal System)
- Device class: 2
- Regulation: 21 CFR 880.5445
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. De Novo decisions do not claim a predicate device.

## Most influential descendants
- K171954: ClearLine IV (2018), 0 descendants of its own

Source page: https://510kreport.com/device/DEN080009
Methodology: https://510kreport.com/methodology