The following data is part of a premarket notification filed by Shanghai Apolo Medical Technology Co., Ltd. with the FDA for Picosecond Nd: Yag Laser System.
Device ID | K200116 |
510k Number | K200116 |
Device Name: | PicoSecond Nd: YAG Laser System |
Classification | Powered Laser Surgical Instrument |
Applicant | Shanghai Apolo Medical Technology Co., Ltd. 4F, Building A, No.388, Yindu Road, Xuhui District Shanghai, CN 200231 |
Contact | Felix Li |
Correspondent | Claire Zhang Shanghai Landlink Medical Information Technology Co., Ltd. Room 703, 705 , Building 1, West Guangzhong Road 555, Jingan District Shanghai, CN 200071 |
Product Code | GEX |
CFR Regulation Number | 878.4810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2020-01-21 |
Decision Date | 2020-05-28 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
06970745912989 | K200116 | 000 |