# K070384: Argon Continuous Flush Device

- Pathway: 510(k) (Traditional)
- Applicant: Argon Medical Devices, Inc.
- Decided: Mar 29, 2007 after 48 days
- Product code: KRA (Catheter, Continuous Flush)
- Device class: 2
- Regulation: 21 CFR 870.1210
- 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 K792141 (1979). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K792141: Continuous Flush Device, Pharmaseal Div., Baxter Healthcare Corp. (1979) Summary page 1.
- K832907: Invasive Monitoring Kits, American Pharmaseal Div. Ahsc (1984) Summary page 1.

## Indications for use
For use in invasive physiological pressure measurements which require continuous regulated flow to maintain catheter patency.

Source page: https://510kreport.com/device/K070384
Methodology: https://510kreport.com/methodology