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 |