Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Ultrasonic Fetal Doppler

K-Number: K233823 · 2024-06-28

Decision Date2024-06-28
Product CodeKNG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Ultrasonic Fetal Doppler is a medical device manufactured by Shenzhen Jamr Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-06-28 under approval number K233823. The device is classified under product code KNG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

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.