Ultrasonic Fetal Doppler
K-Number: K233823 · 2024-06-28
Device Summary
Frequently Asked Questions
What is the Ultrasonic Fetal Doppler?
Ultrasonic Fetal Doppler is a medical device that received FDA 510(k) clearance on 2024-06-28. It is manufactured by Shenzhen Jamr Technology Co., Ltd.. The 510(k) number is K233823.
When was Ultrasonic Fetal Doppler approved by the FDA?
Ultrasonic Fetal Doppler received FDA 510(k) clearance on 2024-06-28, under approval number K233823.
What company makes Ultrasonic Fetal Doppler?
Ultrasonic Fetal Doppler is manufactured by Shenzhen Jamr Technology Co., Ltd..
What is the FDA product code for Ultrasonic Fetal Doppler?
The FDA product code for Ultrasonic Fetal Doppler is KNG.
Related Clinical Trials
Other Devices by Shenzhen Jamr Technology Co., Ltd.
Related Devices (Code: KNG)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.