# K062539: Ncontact Coagulation System Kit

- Pathway: 510(k) (Traditional)
- Applicant: Ncontact Surgical, Inc.
- Decided: Dec 1, 2006 after 94 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- 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: 7 generations back to K942299 (1995). 53 ancestors in all.
No later device cites it as a predicate yet.
0 of 54 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K031247: Cardioblate Bipolar Radiofrequency Surgical Ablation System, Medtronic Vascular (2003) Summary page 1.
- K992972: Arthrocare System 2000 Controller, Arthrocare Cable, Footswitch, Powercord, Arthrocare Electrosurgery Wand, Models H2000, Arthrocare Corp. (1999) Summary page 1.
- K971532: Arthrocare Electrosurgery System, Arthrocare Corp. (1997) Summary page 1.
- K981981: Electrosurgical Unit (Esu) (115 Volt) Model 4810, Electrosurgical Unit (Esu) (230 Volt) Model 4811, Instrument Cable, 19, Boston Scientific Corp (1998) Summary page 1.

## Indications for use
The nContact Coagulation System is intended for the coagulation of soft tissue using Radiofrequency (RF) energy.

Source page: https://510kreport.com/device/K062539
Methodology: https://510kreport.com/methodology