LIGHTSTREAM LOW LEVEL LASER— 510(k) K081166

Substantially Equivalent

Solica Corporation

FDA 510(k) clearance K081166 for LIGHTSTREAM LOW LEVEL LASER, Substantially Equivalent on 2009-04-03. Applicant: Solica Corporation. Device class: 2.

Clearance details

Applicant: Solica Corporation
Product code: Code NHN
Device class: Class 2
Regulation: 21 CFR 890.5500
Advisory panel: Physical Medicine
Date received: 2008-04-24
Decision date: 2009-04-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Toronto, Ontario, CA

Download summary PDF View on FDA.gov ↗

Recent devices under product code NHN

K254024 — MR5 Activ Pro2026-05-19
K251903 — Erchonia DPN Laser (Model# EVRL)2026-02-19
K252273 — Therapy US2025-12-12
K241057 — Enhanced Handheld Pain Relief Laser Instrument (GD-P-E)2025-01-24
K232813 — Therapy EC, Therapy XT2024-12-19

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