# K150993: NICO TRIOwand

- Pathway: 510(k) (Traditional)
- Applicant: Nico Corporation
- Decided: Apr 23, 2015 after 8 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: 3 generations back to K923332 (1992). 6 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K960455: Bipolar Suction Coagulator, Kirwan Surgical Products, Inc. (1996) Summary page 4.
- K992931: Non-Stick Bipolar Forceps, Silverglide Surgical Technologies (1999) Summary page 4.

## Most influential descendants
- K162075: NICO TRIOwand (2016), 0 descendants of its own

## Indications for use
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/K150993
Methodology: https://510kreport.com/methodology