# K162075: NICO TRIOwand

- Pathway: 510(k) (Special)
- Applicant: Nico Corporation
- Decided: Aug 11, 2016 after 15 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: 4 generations back to K923332 (1992). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K150993: NICO TRIOwand, Nico Corporation (2015) Summary page 4.

## Indications for use
The NICO TRIOwand is a disposable device designed to be used in soft tissue surgical procedures that require slow to rapid fluid evacuation and low energy output for the coagulation of tissue.

Source page: https://510kreport.com/device/K162075
Methodology: https://510kreport.com/methodology