The following data is part of a premarket notification filed by Shenzhen Mericonn Technology Co., Ltd. with the FDA for Fetal Doppler.
| Device ID | K212084 | 
| 510k Number | K212084 | 
| Device Name: | Fetal Doppler | 
| Classification | Monitor, Ultrasonic, Fetal | 
| Applicant | Shenzhen Mericonn Technology Co., Ltd. Room 20203, Building 6, Donglongxing Kejiyuan, Huaning Road, Xinshishequ, Dalang Street Shenzhen, CN 518109 | 
| Contact | Jiang Chuanyuan | 
| Correspondent | Kevin Wang Chonconn Medical Device Consulting Co., Ltd. Room 508, Block C, No. 1029 Nanhai Avenue, Nanshan District, Shenzhen, CN 518067  | 
| Product Code | KNG | 
| CFR Regulation Number | 884.2660 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2021-07-02 | 
| Decision Date | 2021-11-03 | 
| Device Identifier | submissionNumber | Supplement | 
|---|---|---|
| 06975725492000 | K212084 | 000 | 
| 00860005571987 | K212084 | 000 | 
| 06975725494004 | K212084 | 000 | 
| 06975725493007 | K212084 | 000 | 
| 06975725491003 | K212084 | 000 | 
Mark Image Registration | Serial  | Company  Trademark Application Date  | 
|---|---|
![]() FETAL DOPPLER  90794910  not registered Live/Pending  | 
        Wu, Jingmei  2021-06-25  |