Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) 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

ApplicantShenzhen Jamr Technology Co., Ltd.
Decision Date2024-06-28
Product CodeKNG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Ultrasonic Fetal Doppler is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Jamr Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-06-28 under 510(k) 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. The listed applicant is Shenzhen Jamr Technology Co., Ltd.. The 510(k) number is K233823.

When did Ultrasonic Fetal Doppler receive FDA 510(k) clearance?

Ultrasonic Fetal Doppler received FDA 510(k) clearance on 2024-06-28, under 510(k) number K233823.

Who is the listed applicant for Ultrasonic Fetal Doppler?

The FDA 510(k) record lists Shenzhen Jamr Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Ultrasonic Fetal Doppler?

The FDA product code for Ultrasonic Fetal Doppler is KNG.

Other records listing Shenzhen Jamr Technology Co., Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253570Blood Pressure Monitor (W06LT)K251331Blood Pressure Monitor (B73, BE23T)K233146Blood Pressure MonitorK230409Wrist Type Blood Pressure Monitor (W05,W1101L)K220886Upper Arm Type Blood Pressure MonitorK200437Blood Pressure Monitor

View all 7 devices →

Related Devices (Code: KNG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K252669Fetal Doppler U8-25, U9-25Zhongshan Xiaolan Town Senlan Electronic FactoryK242846Doppler FHR Detector (BF-500D+, BF-560)Shenzhen Bestman Instrument Co., Ltd.K232893Pocket Fetal Doppler (CONTEC 10D), Pocket Fetal Doppler (CONTEC 10E), Pocket Fetal Doppler (CONTEC 10F)Contec Medical Systems Co.,LtdK220245Pocket Fetal Doppler (Models CONTEC10C and CONTEC10CL)Contec Medical Systems Co.,LtdK211940Fetal DopplerShenzhen Taikang Medical Equipment Co., Ltd.K212084Fetal DopplerShenzhen Mericonn Technology Co., Ltd.

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.

↑