Fetal Doppler

Monitor, Ultrasonic, Fetal

Shenzhen Mericonn Technology Co., Ltd.

The following data is part of a premarket notification filed by Shenzhen Mericonn Technology Co., Ltd. with the FDA for Fetal Doppler.

Pre-market Notification Details

Device IDK212084
510k NumberK212084
Device Name:Fetal Doppler
ClassificationMonitor, Ultrasonic, Fetal
Applicant Shenzhen Mericonn Technology Co., Ltd. Room 20203, Building 6, Donglongxing Kejiyuan, Huaning Road, Xinshishequ, Dalang Street Shenzhen,  CN 518109
ContactJiang Chuanyuan
CorrespondentKevin Wang
Chonconn Medical Device Consulting Co., Ltd. Room 508, Block C, No. 1029 Nanhai Avenue, Nanshan District, Shenzhen,  CN 518067
Product CodeKNG  
CFR Regulation Number884.2660 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2021-07-02
Decision Date2021-11-03

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
06975725492000 K212084 000
00860005571987 K212084 000

Trademark Results [Fetal Doppler]

Mark Image

Registration | Serial
Company
Trademark
Application Date
FETAL DOPPLER
FETAL DOPPLER
90794910 not registered Live/Pending
Wu, Jingmei
2021-06-25

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