# K073400: Varicath Peripheral Infusion Catheter

- Pathway: 510(k) (Special)
- Applicant: Veinrx, Inc.
- Decided: Dec 20, 2007 after 16 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: 6 generations back to K904788 (1990). 11 ancestors in all.
No later device cites it as a predicate yet.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K041517: Infusioncath, Id, LLC (2004) Summary page 1.
- K052738: Infusioncath Peripheral Infusion Catheter, Models VF0012, VF0016, VF0024, VF0028, VF0032, VF0036, VF0040, VF0044, Veinrx, Inc. (2005) Summary page 1.

## Indications for use
The VariCath Peripheral Infusion Catheter is intended for infusion of physician specified fluids, including thrombolytics, into the peripheral vasculature.

Source page: https://510kreport.com/device/K073400
Methodology: https://510kreport.com/methodology