# K071959: Angiodynamics, Inc.Nevertouch 600UM Fiber and Venacure Procedure Kit

- Pathway: 510(k) (Special)
- Applicant: AngioDynamics, Inc.
- Decided: Aug 1, 2007 after 16 days
- Product code: GEX (Powered Laser Surgical Instrument)
- Device class: 2
- Regulation: 21 CFR 878.4810
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K140458: Diotech Laser Fiber (2014), 1 descendant of its own
- K152667: ATOVEN-Reusable Laser Fiber (2016), 0 descendants of its own
- K073464: Angiodynamics, Inc., Nevertouch II 400UM Fiber and Venacure Procedure Kit (2008), 0 descendants of its own

## Indications for use
The AngioDynamics, Inc. NeverTouch 600gm Fiber is indicated for endovascular coagulation of the great saphenous vein in patients with superficial vein reflux, for the treatment of varicose veins and varicosities associated with superficial reflux of the great saphenous vein, and for the treatment of incompetence and reflux of superficial veins of the lower extremity.

Source page: https://510kreport.com/device/K071959
Methodology: https://510kreport.com/methodology