QUASAR BLUE LIGHT THERAPY SYSTEM— 510(k) K093963

Name: FDA 510(k) clearance K093963
Creator: U.S. Food and Drug Administration
Published: 2010-08-27

Substantially Equivalent

Silver Bay, LLC

FDA 510(k) clearance K093963 for QUASAR BLUE LIGHT THERAPY SYSTEM, Substantially Equivalent on 2010-08-27. Applicant: Silver Bay, LLC. Device class: 2.

Clearance details

Applicant: Silver Bay, LLC
Product code: Code OLP
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 2009-12-23
Decision date: 2010-08-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sarasota, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code OLP

view all

K253878 — LUSTRE GoGlow Advanced LED Patches (PR8001, PR9001)2026-03-04
K251843 — Erchonia EVRL2025-09-12
K242068 — LED Light Therapy Mask (RT01)2025-04-04
K243555 — LED light therapy mask (E43, E32, E49B, E49C, E100B, E100C, E103B, E104B, E106A, E108A)2025-02-05
K232656 — BLU TOTALE (Model: ENEOB852)2023-11-14

More clearances from Silver Bay, LLC

view all

K112362 — C100 WRINKLE REDUCTION DEVICE2012-08-14
K111286 — QUASAR CALYPSO2012-01-18
K091467 — BABY QUASAR2010-09-17
K072767 — QUASAR BLUE LIGHT THERAPY SYSTEM2007-10-15

Adverse events under product code OLP

product code OLP

Other: 1
Total: 1

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.