LITECURE THERAPY SYSTEM MODEL LTS-1500— 510(k) K123014

Name: FDA 510(k) clearance K123014
Creator: U.S. Food and Drug Administration
Published: 2013-03-29

Substantially Equivalent

Litecure, LLC

FDA 510(k) clearance K123014 for LITECURE THERAPY SYSTEM MODEL LTS-1500, Substantially Equivalent on 2013-03-29. Applicant: Litecure, LLC. Device class: 2.

Clearance details

Applicant: Litecure, LLC
Product code: Code PDZ
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 2012-09-27
Decision date: 2013-03-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Newark, DE, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code PDZ

view all

K253960 — Medicell Mycosis Laser (MCML24004)2026-03-09
K241116 — Onycho Laser V2024-07-22
K211265 — TFX-LT2000 Therapy Light2022-11-17
K221363 — AF Laser2022-07-20
K190034 — REMY Medical Therapy Laser System2019-05-15

More clearances from Litecure, LLC

view all

K173067 — LightForce LTS Model 1000, 1500, 2500, and 40002018-02-22
K123031 — BWF-5 MEDICAL LASER SERIES2012-12-03
K121487 — LITECURE THERAPY COMPACT2012-06-12
K103511 — LITECURE THERAPY SYSTEM2011-01-25
K093087 — BWF-5 MEDICAL LASER SERIES2010-05-12

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