NUVO VERDE LED LIGHTING SYSTEM— 510(k) K083323

Name: FDA 510(k) clearance K083323
Creator: U.S. Food and Drug Administration
Published: 2009-01-28

Substantially Equivalent

Nuvo, Inc.

FDA 510(k) clearance K083323 for NUVO VERDE LED LIGHTING SYSTEM, Substantially Equivalent on 2009-01-28. Applicant: Nuvo, Inc.. Device class: 2.

Clearance details

Applicant: Nuvo, Inc.
Product code: Code FSY
Device class: Class 2
Regulation: 21 CFR 878.4580
Advisory panel: General, Plastic Surgery
Date received: 2008-11-12
Decision date: 2009-01-28
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Erie, PA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FSY

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K142984 — Leo Minor2014-10-29
K142076 — CLAVEGUARD FREEDOM SURGICAL LIGHT2014-09-30
K140812 — MI-750 PROCEDURAL/MINOR SURGICAL LIGHT2014-08-07
K132551 — ZF 7202014-06-30
K140930 — VIDA LED SURGICAL LIGHTING SYSTEM, V SERIES2014-06-09

Adverse events under product code FSY

product code FSY

Malfunction: 2,759
Other: 1
Total: 2,760

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.