# K090661: Nes Reprocessed Varicose Vein RF Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Northeast Scientific, Inc.
- Decided: Jul 21, 2010 after 496 days
- Product code: NUJ (Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 9 generations back to K943450 (1995). 24 ancestors in all.
No later device cites it as a predicate yet.
0 of 25 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K061373: Vnus Closurefast Catheter, Models CF7-7-60 and CF7-7-100, Vnus Medical Technologies, Inc. (2006) Summary page 1.

## Indications for use
The NES Reprocessed Varicose Vein RF Catheter is intended for endovascular coagulation of blood vessels in patients with superficial vein reflux

Source page: https://510kreport.com/device/K090661
Methodology: https://510kreport.com/methodology