ATL Angelite-DDC

• FDA 510(k) K083915 decided 29 Jan 2009 Active
• FDA GUDID UDI-DI 06970507240022 listed 20 Oct 2016 Listed

1. 29 Jan 2009 Cleared FDA 510(k) K083915
2. 20 Oct 2016 Listed FDA GUDID 06970507240022

Trade name

Atl

Generic name

Intense pulsed light skin surface treatment system

Model / reference

Angelite-DDC

Primary DI / UDI-DI

06970507240022

510(k) Number

K083915 ↗

FDA product code

GEX

GMDN term

Intense pulsed light skin surface treatment system

Device class

Class II

Regulation number

878.4810

GUDID distribution status

In Commercial Distribution

MRI safety

MR Unsafe

Category: Intense pulsed light skin surface treatment system

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• Atl Atl-150

  Class II

  FDA 510(k) K083918 Active Cleared 2 Feb 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. →