510(k) K040480

Device
SONOTRAX ULTRASONIC POCKET DOPPLER
Applicant
EDAN INSTRUMENTS, INC.
510(k) number
K040480
Product code
KNG  
Decision
Substantially Equivalent (SESE)
Decision date
2004-05-25
Date received
2004-02-25
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
Summary
Third party reviewed
No

Applicant Contact#

Contact
WILLIAM STERN
Address
1 Odell Plz. Yonkers NY US 10701 10701

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code KNG  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K252669Fetal Doppler U8-25, U9-25Zhongshan Xiaolan Town Senlan Electronic Factory2026-01-08
K242846Doppler FHR Detector (BF-500D+, BF-560)Shenzhen Bestman Instrument Co., Ltd.2025-06-26
K233823Ultrasonic Fetal DopplerShenzhen Jamr Technology Co., Ltd.2024-06-28
K232893Pocket Fetal Doppler (CONTEC 10D), Pocket Fetal Doppler (CONTEC 10E), Pocket Fetal Doppler (CONTEC 10F)Contec Medical Systems Co.,Ltd2024-06-14
K220245Pocket Fetal Doppler (Models CONTEC10C and CONTEC10CL)Contec Medical Systems Co.,Ltd2022-09-28
K211940Fetal DopplerShenzhen Taikang Medical Equipment Co., Ltd.2022-01-07
K212084Fetal DopplerShenzhen Mericonn Technology Co., Ltd.2021-11-03
K191110HeraBEAT™ USHeramed, Ltd.2019-11-14
K182526Fetal Doppler (Models: FD-231B, FD-231D, FD-640B, FD-640D, FD-200B, FD-200D, FD-591B, and FD-591D)Vcomin Technology Limited2019-05-29
K182710Fetal Doppler, Model FD88Shenzzhen Luckcome Technology Inc., Ltd.2019-03-01
K182190Fetal DopplerShenzhen AOJ Medical Technology Co., Ltd.2018-12-19
K180419Ultrasonic Doppler (Model YM-2T8)Shenzhen Imdk Medical Technology Co., Ltd.2018-07-19
K172780SD1 Ultrasonic Pocket DopplerEdan Instruments, Inc.2018-06-06
K153475SD5 & SD6 Ultrasonic Tabletop DopplerEdan Instruments, Inc.2016-01-29
K140579ULTRASONIC POCKET DOPPLEREdan Instruments, Inc.2015-02-06

Legacy Summary#

summary

FDA Review#

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