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Monitor, Ultrasonic, Fetal

FDA product code KNG · Class 2 · Obstetrics/Gynecology

287
Registered devices
32
Adverse events
1
Recalls
60
510(k) clearances

Devices with this code

FaceLake — LORTE TECHNOLOGIES, INCNeeva Baby — Sebe IncClearTone Doppler — Coopersurgical, Inc.CONTEC — Contec Medical Systems Co., Ltd.ES102EX — KOVEN TECHNOLOGY, INC.Care Mill — SIMPROClearTone Doppler — Coopersurgical, Inc.FaceLake — LORTE TECHNOLOGIES, INCTRIA II — Coopersurgical, Inc.DOPPLEX — HUNTLEIGH HEALTHCARE LIMITEDBaby Doppler — DAGAMMA INC.MedOne — MEDONE LLCImex 8MHZ DOPPLER PROBE, PD2 — IMEX, LLCMediChoice — Coopersurgical, Inc.SpringBud Fetal Doppler — Vcomin Technlogy LimitedMediChoice — Coopersurgical, Inc.VCOMIN Fetal Doppler — Vcomin Technlogy LimitedSummit Doppler — Coopersurgical, Inc.Tenovi — Tenovi Co.2.0 MHz Waterproof Obstetrical Probe — Coopersurgical, Inc.McKesson — MCKESSON MEDICAL-SURGICAL INC.Summit Doppler — Coopersurgical, Inc.Jumper — Shenzhen Jumper Medical Equipment Co.,Ltd.IMDK — Shenzhen IMDK Medical Technology Co., Ltd

Recent recalls

DateFirmReason
2017-10-06CooperSurgical, Inc.The 2MHZ prove was incorrectlhttp://cts.fda.gov/division-tracking/images/trash.pngy labeled as a 3MHZ probe

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.