The following data is part of a premarket notification filed by Beijing Adss Development Co., Ltd with the FDA for Nd Yag Q-switch Laser Therapy Machine.
Device ID | K161926 |
510k Number | K161926 |
Device Name: | ND YAG Q-switch Laser Therapy Machine |
Classification | Powered Laser Surgical Instrument |
Applicant | Beijing ADSS Development Co., Ltd F6, Xiandao Bldg., Jinyuan Rd. 36 Daxing Economic Development Zone Beijing, CN 102628 |
Contact | Gao Yurong |
Correspondent | Ray Wang Beijing Believe Technology Service Co., Ltd. 5-1206, Build 332, DaFangJu No.25 BanBiDian Rd. Liyuan Town, Tongzhou District, Beijing, CN 101121 |
Product Code | GEX |
CFR Regulation Number | 878.4810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2016-07-13 |
Decision Date | 2017-02-22 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
06970453270142 | K161926 | 000 |
06970453270135 | K161926 | 000 |
06970453270012 | K161926 | 000 |