510(k) K233823

Device
Ultrasonic Fetal Doppler
Applicant
Shenzhen Jamr Technology Co., Ltd.
510(k) number
K233823
Product code
KNG
Decision
Substantially Equivalent (SESE)
Decision date
2024-06-28
Date received
2023-12-01
Regulation
884.2660
Classification name
Monitor, Ultrasonic, Fetal
Medical specialty
Obstetrics/Gynecology
Review panel
Obstetrics/Gynecology
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No

Applicant Contact#

Contact
Haiyu Zhang
Address
A101-301, D101-201, Jamr Science & Technology Park, #2 Guiyuan Rd., Guixiang Community Shenzhen CN 518100 518100

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code KNG#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
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