Advanced Technology Laser Co., Ltd. is one of 2152 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Advanced Technology Laser Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: LONG PULSE ND: YAG LASER SYSTEM, CO2 LASER SYSTEM, Q-SWITCHED ND:YAG LASER SYSTEM, MODEL GLOBALCURE-SC6
5
Total
5
Cleared
0
Denied
Advanced Technology Laser Co., Ltd. has 5 FDA 510(k) cleared medical devices. Based in Shanghai, CN.
Historical record: 5 cleared submissions from 2009 to 2014. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Advanced Technology Laser Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Advanced Technology Laser Co., Ltd.
5 devices
Cleared
Oct 08, 2014
LONG PULSE ND: YAG LASER SYSTEM
General & Plastic Surgery
250d
Cleared
Sep 17, 2010
CO2 LASER SYSTEM
General & Plastic Surgery
105d
Cleared
Jul 29, 2010
Q-SWITCHED ND:YAG LASER SYSTEM, MODEL GLOBALCURE-SC6
General & Plastic Surgery
8d
Cleared
Feb 02, 2009
ATL CO2 MEDICAL LASER SYSTEMS, MODELS ATL-150 AND ATL-250
General & Plastic Surgery
34d
Cleared
Jan 29, 2009
ANGELITE FAMILY OF INTENSE PULSED LIGHT SYSTEMS, MODELS ANGELITE-DDC AND...
General & Plastic Surgery
30d