FETAL DOPPLER JPD-100S— 510(k) K110124

Name: FDA 510(k) clearance K110124
Creator: U.S. Food and Drug Administration
Published: 2011-02-04

Substantially Equivalent

Shenzhen Jumper Medical Equipment Co., Ltd.

FDA 510(k) clearance K110124 for FETAL DOPPLER JPD-100S, Substantially Equivalent on 2011-02-04. Applicant: Shenzhen Jumper Medical Equipment Co., Ltd.. Device class: 2.

Clearance details

Applicant: Shenzhen Jumper Medical Equipment Co., Ltd.
Product code: Code KNG
Device class: Class 2
Regulation: 21 CFR 884.2660
Advisory panel: Obstetrics/Gynecology
Date received: 2011-01-18
Decision date: 2011-02-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shanghai, CN

Download summary PDF View on FDA.gov ↗

Recent devices under product code KNG

view all

K252669 — Fetal Doppler U8-25, U9-252026-01-08
K242846 — Doppler FHR Detector (BF-500D+, BF-560)2025-06-26
K233823 — Ultrasonic Fetal Doppler2024-06-28
K232893 — Pocket Fetal Doppler (CONTEC 10D), Pocket Fetal Doppler (CONTEC 10E), Pocket Fetal Doppler (CONTEC 10F)2024-06-14
K220245 — Pocket Fetal Doppler (Models CONTEC10C and CONTEC10CL)2022-09-28

More clearances from Shenzhen Jumper Medical Equipment Co., Ltd.

view all

K231310 — Electronic Blood Pressure Monitor2023-10-27
K182871 — Mini TENS Therapy Device2019-08-01
K182437 — Wireless Intelligent Thermometer2019-05-05
K182495 — Electronic Blood Pressure Monitor2019-03-03
K172795 — Infrared Thermometer2018-03-14

Data sourced from openFDA. This site is unofficial and independent of the FDA.