# K083323: Nuvo Verde Led Lighting System

- Pathway: 510(k) (Abbreviated)
- Applicant: Nuvo, Inc.
- Decided: Jan 28, 2009 after 77 days
- Product code: FSY (Light, Surgical, Ceiling Mounted)
- Device class: 2
- Regulation: 21 CFR 878.4580
- 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 K965130 (1997). 10 ancestors in all.
No later device cites it as a predicate yet.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K071698: Aurora Led Series Surgical Lights, Skytron, Div. the Kmw Group, Inc. (2007) Summary page 1.
- K072072: Harmony Led-1 Surgical Lighting System, STERIS Corporation (2007) Summary page 1.
- K061317: ILED, Trumpf Kreuzer Medizin Systeme GmbH + Co.Kg (2006) Summary page 1.

## Indications for use
The Verde LED Surgical Light System, subjected in-this submission is a variable pattern / intensity surgical light designed to provide illumination of the surgical field and patient during surgical and non-surgical procedures.

Source page: https://510kreport.com/device/K083323
Methodology: https://510kreport.com/methodology