Atl Atl-150

• FDA 510(k) K083918 decided 2 Feb 2009 Active
• FDA GUDID UDI-DI 06970507240107 listed 26 Oct 2016 Listed

1. 2 Feb 2009 Cleared FDA 510(k) K083918
2. 26 Oct 2016 Listed FDA GUDID 06970507240107

Trade name

Atl

Generic name

Dermatological carbon dioxide laser system

Model / reference

ATL-150

Primary DI / UDI-DI

06970507240107

510(k) Number

K083918 ↗

FDA product code

GEX

GMDN term

Dermatological carbon dioxide laser system

Device class

Class II

Regulation number

878.4810

GUDID distribution status

In Commercial Distribution

MRI safety

MR Unsafe

Category: Dermatological carbon dioxide laser system

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• Model 545-45 Laser for Derma., Pod., Surgical by Britt Corp., Inc.
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• Model 1210 OmniPulse Holmium Laser System by TRIMEDYNE, INC.
• Fencer 308 Excimer Laser System by Kera Harvest/Laser Max Medical Technologies Corp

• ATL Angelite-DDC

  Class II

  FDA 510(k) K083915 Active Cleared 29 Jan 2009 GUDID on market

• ATL GlobalCure-SC6

  Class II

  FDA 510(k) K102050 Active Cleared 29 Jul 2010 GUDID on market

• Atl Atl-250

  Class II

  FDA 510(k) K083918 Active Cleared 2 Feb 2009 GUDID on market

• ATL eBeam

  Class II

  FDA 510(k) K101555 Active Cleared 17 Sep 2010 GUDID on market

See all devices from Advanced Technology Laser Co., Ltd. →