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 |